A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666995



Internal ID18965276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13651220..13842119hg38UCSC Ensembl
Innerchr8:13508729..13699628hg19UCSC Ensembl
Innerchr8:13553100..13743999hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38190900
hg19190900
hg18190900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017083
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3666995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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