A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663114



Internal ID15399766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110836356..110845101hg38UCSC Ensembl
Innerchr1:111378978..111387723hg19UCSC Ensembl
Innerchr1:111180501..111189246hg18UCSC Ensembl
Innerchr1:111091020..111099765hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg388746
hg198746
hg188746
hg178746
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517082
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663114
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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