A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704696



Internal ID15441348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6278786..6280383hg38UCSC Ensembl
Innerchr11:6300016..6301613hg19UCSC Ensembl
Innerchr11:6256592..6258189hg18UCSC Ensembl
Innerchr11:6256592..6258189hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381598
hg191598
hg181598
hg171598
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528149
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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