A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685334



Internal ID18636929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20986290..21073448hg38UCSC Ensembl
Innerchr8:20843801..20930959hg19UCSC Ensembl
Innerchr8:20888081..20975239hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3887159
hg1987159
hg1887159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028279
Supporting Variants
Samples
Known GenesLOC286114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685334
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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