A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148932



Internal ID15877517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105580652..105655000hg38UCSC Ensembl
Innerchr13:106233001..106307349hg19UCSC Ensembl
Innerchr13:105031002..105105350hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3874349
hg1974349
hg1874349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563005
Supporting Variants
SamplesHGDP01001
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148932
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