A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005797



Internal ID22067428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65445150..65480454hg38UCSC Ensembl
Outerchr10:65443747..65483619hg38UCSC Ensembl
Innerchr10:67204908..67240212hg19UCSC Ensembl
Outerchr10:67203505..67243377hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3839873
hg1939873
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154612
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005797
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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