A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585269



Internal ID18883550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13193869..13703148hg38UCSC Ensembl
Innerchr21:14566190..15075469hg19UCSC Ensembl
Innerchr21:13488061..13997340hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38509280
hg19509280
hg18509280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060462
Supporting Variants
Samples
Known GenesLOC100288966, MIR3156-3, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585269
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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