A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691492



Internal ID18989773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:122486276..122544409hg38UCSC Ensembl
Innerchr8:123498515..123556648hg19UCSC Ensembl
Innerchr8:123567696..123625829hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3858134
hg1958134
hg1858134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026013
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)nssv3691492
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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