A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681781



Internal ID18633376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12077151..12620670hg38UCSC Ensembl
Innerchr8:11934660..12478179hg19UCSC Ensembl
Innerchr8:11972069..12522550hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38543520
hg19543520
hg18550482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018090
Supporting Variants
Samples
Known GenesDEFB109P1, DEFB130, FAM66A, FAM66D, FAM86B1, FAM86B2, FAM90A25P, FAM90A2P, LOC100133267, LOC100506990, LOC392196, LOC649352, LOC729732, USP17L2, USP17L7, ZNF705D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681781
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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