A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691531



Internal ID18989812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131610699..131647181hg38UCSC Ensembl
Innerchr8:132622946..132659428hg19UCSC Ensembl
Innerchr8:132692128..132728610hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3836483
hg1936483
hg1836483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017607
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)nssv3691531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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