A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599818



Internal ID18898099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19160797..19217111hg38UCSC Ensembl
Innerchr21:20533115..20589428hg19UCSC Ensembl
Innerchr21:19454986..19511299hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3856315
hg1956314
hg1856314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060710
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)nssv3599818
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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