A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006266



Internal ID18748797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70951490..70992460hg38UCSC Ensembl
Innerchr1:71417173..71458143hg19UCSC Ensembl
Innerchr1:71189761..71230731hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3840971
hg1940971
hg1840971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n100
Supporting Variantsnssv3466792
Samples
Known GenesPTGER3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006266
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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