A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698820



Internal ID15435472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111384542..111391682hg38UCSC Ensembl
Innerchr1:111927164..111934304hg19UCSC Ensembl
Innerchr1:111728687..111735827hg18UCSC Ensembl
Innerchr1:111639206..111646346hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg387141
hg197141
hg187141
hg177141
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523120
Supporting Variants
Samples
Known GenesPGCP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698820
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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