A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059916



Internal ID19149135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18682133..18706170hg38UCSC Ensembl
Innerchr21:20054451..20078488hg19UCSC Ensembl
Innerchr21:18976322..19000359hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3824038
hg1924038
hg1824038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599684
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)nsv1059916
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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