A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587357



Internal ID16374766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30365391..30454545hg38UCSC Ensembl
Innerchr21:31737709..31826863hg19UCSC Ensembl
Innerchr21:30659580..30748734hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3889155
hg1989155
hg1889155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946600
Samples
Known GenesKRTAP13-1, KRTAP13-2, KRTAP13-3, KRTAP13-4, KRTAP15-1, MIR4327
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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