A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3665724



Internal ID18964005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12387671..12500660hg38UCSC Ensembl
Innerchr8:12245180..12358169hg19UCSC Ensembl
Innerchr8:12289551..12402540hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38112990
hg19112990
hg18112990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027641
Supporting Variants
Samples
Known GenesDEFB109P1, FAM66A, 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)nssv3665724
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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