A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705952



Internal ID15095918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93497971..93506741hg38UCSC Ensembl
Innerchr11:93231137..93239907hg19UCSC Ensembl
Innerchr11:92870785..92879555hg18UCSC Ensembl
Innerchr11:92870785..92879555hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388771
hg198771
hg188771
hg178771
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522568
Supporting Variants
Samples
Known GenesSMCO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705952
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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