A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156768



Internal ID22087169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157545672..157558146hg38UCSC Ensembl
Outerchr7:157544783..157559061hg38UCSC Ensembl
Innerchr7:157338366..157350840hg19UCSC Ensembl
Outerchr7:157337477..157351755hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3814279
hg1914279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021829, nssv4021827, nssv4021830, nssv4021831, nssv4021817, nssv4021826, nssv4021821, nssv4021825, nssv4021816, nssv4021815, nssv4021819, nssv4021824, nssv4021822, nssv4021828, nssv4021823, nssv4021818, nssv4021820
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156768
Frequency
Sample Size131
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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