A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959136



Internal ID16253092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13044831..13094075hg38UCSC Ensembl
Innerchr3:13086331..13135575hg19UCSC Ensembl
Innerchr3:13061331..13110575hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3849245
hg1949245
hg1849245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589724
Supporting Variants
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959136
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