A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661236



Internal ID18959517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47057928..47089824hg38UCSC Ensembl
Innerchr7:47097526..47129422hg19UCSC Ensembl
Innerchr7:47064051..47095947hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3831897
hg1931897
hg1831897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016441
Supporting Variants
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)nssv3661236
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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