A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660769



Internal ID15050735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125209386..125214846hg38UCSC Ensembl
Innerchr11:125079282..125084742hg19UCSC Ensembl
Innerchr11:124584492..124589952hg18UCSC Ensembl
Innerchr11:124584492..124589952hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385461
hg195461
hg185461
hg175461
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517656
Supporting Variants
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660769
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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