A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005731



Internal ID18748262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26075247..26111305hg38UCSC Ensembl
Innerchr4:26076869..26112927hg19UCSC Ensembl
Innerchr4:25685967..25722025hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3836059
hg1936059
hg1836059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620611
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005731
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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