A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156764



Internal ID22087165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154601461..154609123hg38UCSC Ensembl
Outerchr7:154598185..154609307hg38UCSC Ensembl
Innerchr7:154393171..154400833hg19UCSC Ensembl
Outerchr7:154389895..154401017hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3811123
hg1911123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019747, nssv4019748, nssv4019786, nssv4019782, nssv4021772, nssv4019758, nssv4019734, nssv4019740, nssv4021790, nssv4019781, nssv4019755, nssv4019765, nssv4019798, nssv4019785, nssv4019777, nssv4021771, nssv4021765, nssv4021784, nssv4019745, nssv4019780, nssv4019757, nssv4019753, nssv4021787, nssv4019771, nssv4021775, nssv4019791, nssv4021778, nssv4019744, nssv4021789, nssv4021768, nssv4019735, nssv4021767, nssv4019739, nssv4019752, nssv4019773, nssv4019759, nssv4019764, nssv4019741, nssv4021783, nssv4019750, nssv4019743, nssv4021780, nssv4019784, nssv4021788, nssv4019767, nssv4019774, nssv4021792, nssv4019800, nssv4019799, nssv4021786, nssv4021777, nssv4019772, nssv4019742, nssv4021757, nssv4019751, nssv4019778, nssv4021760, nssv4021781, nssv4021776, nssv4019797, nssv4019738, nssv4019792, nssv4019790, nssv4021769, nssv4019760, nssv4021791, nssv4019761, nssv4019746, nssv4019783, nssv4019762, nssv4019789, nssv4021758, nssv4019788, nssv4019770, nssv4021761, nssv4021779, nssv4019776, nssv4019736, nssv4021759, nssv4019749, nssv4021782, nssv4019769, nssv4019756, nssv4019793, nssv4021774, nssv4019796, nssv4019754, nssv4021763, nssv4021785, nssv4019768, nssv4021766, nssv4019763, nssv4021770, nssv4019737, nssv4019794, nssv4019779, nssv4019766, nssv4021762, nssv4019775, nssv4019787, nssv4021773, nssv4019795, nssv4021764
Samples
Known GenesDPP6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156764
Frequency
Sample Size131
Observed Gain1
Observed Loss102
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer