A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691535



Internal ID18989816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131665346..131704512hg38UCSC Ensembl
Innerchr8:132677593..132716759hg19UCSC Ensembl
Innerchr8:132746775..132785941hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3839167
hg1939167
hg1839167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021083
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)nssv3691535
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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