A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066591



Internal ID19155810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32042851..32098317hg38UCSC Ensembl
Innerchr21:33415164..33470630hg19UCSC Ensembl
Innerchr21:32337035..32392501hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3855467
hg1955467
hg1855467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4425n100
Supporting Variantsnssv3600124, nssv3732696, nssv3600125
Samples
Known GenesLINC00159
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066591
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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