A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685335



Internal ID18983616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21166080..21184667hg38UCSC Ensembl
Innerchr8:21023591..21042178hg19UCSC Ensembl
Innerchr8:21067871..21086458hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3818588
hg1918588
hg1818588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023459
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)nssv3685335
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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