A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701579



Internal ID15091545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125391855..125396997hg38UCSC Ensembl
Innerchr11:125261751..125266893hg19UCSC Ensembl
Innerchr11:124766961..124772103hg18UCSC Ensembl
Innerchr11:124766961..124772103hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385143
hg195143
hg185143
hg175143
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525451
Supporting Variants
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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