A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057359



Internal ID19146578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19160797..19210959hg38UCSC Ensembl
Innerchr21:20533115..20583277hg19UCSC Ensembl
Innerchr21:19454986..19505148hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3850163
hg1950163
hg1850163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4395n100
Supporting Variantsnssv3599817
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)nsv1057359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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