A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585217



Internal ID18883498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:12992198..13028681hg38UCSC Ensembl
Innerchr21:14364519..14401002hg19UCSC Ensembl
Innerchr21:13286390..13322873hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3836484
hg1936484
hg1836484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061116
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)nssv3585217
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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