A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681029



Internal ID18632624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7894514..7930248hg38UCSC Ensembl
Innerchr8:7752036..7787770hg19UCSC Ensembl
Innerchr8:7789446..7825180hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3835735
hg1935735
hg1835735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020139
Supporting Variants
Samples
Known GenesDEFB4A, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681029
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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