A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3680436



Internal ID18632031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7477475..7541364hg38UCSC Ensembl
Innerchr8:7334997..7398886hg19UCSC Ensembl
Innerchr8:7322407..7386296hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3863890
hg1963890
hg1863890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020012
Supporting Variants
Samples
Known GenesDEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, PRR23D1, PRR23D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3680436
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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