A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697520



Internal ID18995801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81110338..81377259hg38UCSC Ensembl
Innerchr9:83725253..83992174hg19UCSC Ensembl
Innerchr9:82915073..83181994hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38266922
hg19266922
hg18266922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052517
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)nssv3697520
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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