A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666846



Internal ID15056812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70970573..71002810hg38UCSC Ensembl
Innerchr1:71436256..71468493hg19UCSC Ensembl
Innerchr1:71208844..71241081hg18UCSC Ensembl
Innerchr1:71148277..71180514hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3832238
hg1932238
hg1832238
hg1732238
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516212
Supporting Variants
Samples
Known GenesPTGER3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666846
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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