A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059156



Internal ID19148375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20202981..20276862hg38UCSC Ensembl
Innerchr21:21575294..21649174hg19UCSC Ensembl
Innerchr21:20497165..20571045hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3873882
hg1973881
hg1873881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4397n100
Supporting Variantsnssv3599831
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)nsv1059156
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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