A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704798



Internal ID15094764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125302778..125305585hg38UCSC Ensembl
Innerchr11:125172674..125175481hg19UCSC Ensembl
Innerchr11:124677884..124680691hg18UCSC Ensembl
Innerchr11:124677884..124680691hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382808
hg192808
hg182808
hg172808
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528236
Supporting Variants
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704798
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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