A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587486



Internal ID16374895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39860633..39882530hg38UCSC Ensembl
Innerchr21:41232560..41254456hg19UCSC Ensembl
Innerchr21:40154430..40176326hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3821898
hg1921897
hg1821897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946782
Samples
Known GenesPCP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587486
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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