A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702965



Internal ID15439617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15204641..15206443hg38UCSC Ensembl
Innerchr11:15226187..15227989hg19UCSC Ensembl
Innerchr11:15182763..15184565hg18UCSC Ensembl
Innerchr11:15182763..15184565hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381803
hg191803
hg181803
hg171803
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516403
Supporting Variants
Samples
Known GenesINSC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702965
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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