A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587077



Internal ID16374486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:16405646..16453940hg38UCSC Ensembl
Innerchr21:17777966..17826260hg19UCSC Ensembl
Innerchr21:16699837..16748131hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3848295
hg1948295
hg1848295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv945514
Samples
Known GenesLINC00478
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587077
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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