A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701973



Internal ID15091939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16013965..16030006hg38UCSC Ensembl
Innerchr1:16340460..16356501hg19UCSC Ensembl
Innerchr1:16213047..16229088hg18UCSC Ensembl
Innerchr1:16085766..16101807hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816042
hg1916042
hg1816042
hg1716042
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517651
Supporting Variants
Samples
Known GenesCLCNKA, HSPB7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701973
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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