A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702286



Internal ID15092252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108930432..108941353hg38UCSC Ensembl
Innerchr1:109473054..109483975hg19UCSC Ensembl
Innerchr1:109274577..109285498hg18UCSC Ensembl
Innerchr1:109185096..109196017hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810922
hg1910922
hg1810922
hg1710922
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526049
Supporting Variants
Samples
Known GenesCLCC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702286
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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