A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587562



Internal ID16028285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41732924..41760723hg38UCSC Ensembl
Innerchr21:43153084..43180883hg19UCSC Ensembl
Innerchr21:42026153..42053952hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3827800
hg1927800
hg1827800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152409
Samples1780862565_A
Known GenesMIR6814, RIPK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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