A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703203



Internal ID15439855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34603692..34611225hg38UCSC Ensembl
Innerchr11:34625239..34632772hg19UCSC Ensembl
Innerchr11:34581815..34589348hg18UCSC Ensembl
Innerchr11:34581815..34589348hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387534
hg197534
hg187534
hg177534
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526845
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703203
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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