A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv734680



Internal ID16028636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201209342..201210692hg38UCSC Ensembl
Innerchr1:201178470..201179820hg19UCSC Ensembl
Innerchr1:199445093..199446443hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381351
hg191351
hg181351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548992
Supporting Variants
Samples
Known GenesIGFN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv734680
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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