A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3665901



Internal ID18964182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12519957hg38UCSC Ensembl
Innerchr8:12260915..12377466hg19UCSC Ensembl
Innerchr8:12305286..12421837hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38116552
hg19116552
hg18116552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031872
Supporting Variants
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3665901
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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