A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056645



Internal ID19145864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19943504..20091287hg38UCSC Ensembl
Innerchr21:21315818..21463600hg19UCSC Ensembl
Innerchr21:20237689..20385471hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38147784
hg19147783
hg18147783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599827
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)nsv1056645
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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