A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3663726



Internal ID18962007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12376119..12454117hg38UCSC Ensembl
Innerchr8:12233628..12311626hg19UCSC Ensembl
Innerchr8:12277999..12355997hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3877999
hg1977999
hg1877999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022828
Supporting Variants
Samples
Known GenesDEFB109P1, FAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC649352
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3663726
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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