A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946767



Internal ID16240723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36964896..37000429hg38UCSC Ensembl
Innerchr21:38337196..38372729hg19UCSC Ensembl
Innerchr21:37259066..37294599hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3835534
hg1935534
hg1835534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587471
Supporting Variants
Samples
Known GenesHLCS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer