A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599977



Internal ID18898258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:23026821..23386261hg38UCSC Ensembl
Innerchr21:24399143..24758582hg19UCSC Ensembl
Innerchr21:23321014..23680453hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38359441
hg19359440
hg18359440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056792
Supporting Variants
Samples
Known GenesD21S2088E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599977
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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