A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967757



Internal ID16261713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90215618..90342524hg38UCSC Ensembl
Innerchr3:90264768..90391674hg19UCSC Ensembl
Innerchr3:90347458..90474364hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38126907
hg19126907
hg18126907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590972
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967757
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