A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599888



Internal ID18898169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:22198149..22674806hg38UCSC Ensembl
Innerchr21:23570468..24047126hg19UCSC Ensembl
Innerchr21:22492339..22968997hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38476658
hg19476659
hg18476659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064068
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)nssv3599888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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