A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3753694



Internal ID18705289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7545386..8105114hg38UCSC Ensembl
Innerchr8:7402908..7962636hg19UCSC Ensembl
Innerchr8:7390318..8000046hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38559729
hg19559729
hg18609729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023541
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4A, FAM66E, FAM90A10P, FAM90A7P, MIR548I3, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L3, USP17L8, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3753694
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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