A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004507



Internal ID22066138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112352317..112357081hg38UCSC Ensembl
Outerchr10:112351590..112358659hg38UCSC Ensembl
Innerchr10:114112075..114116839hg19UCSC Ensembl
Outerchr10:114111348..114118417hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg387070
hg197070
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154656
Supporting Variants
Samples
Known GenesGUCY2GP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004507
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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