A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673778



Internal ID15410430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63070597..63072195hg38UCSC Ensembl
Innerchr11:62838069..62839667hg19UCSC Ensembl
Innerchr11:62594645..62596243hg18UCSC Ensembl
Innerchr11:62594645..62596243hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
hg171599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517447
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673778
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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