A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703313



Internal ID15093279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109741130..109769537hg38UCSC Ensembl
Innerchr13:110393477..110421884hg19UCSC Ensembl
Innerchr13:109191478..109219885hg18UCSC Ensembl
Innerchr13:109191478..109219885hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3828408
hg1928408
hg1828408
hg1728408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526943
Supporting Variants
Samples
Known GenesIRS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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