A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004587



Internal ID22066218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8831330..8969912hg38UCSC Ensembl
Outerchr10:8827870..8972023hg38UCSC Ensembl
Innerchr10:8873293..9011875hg19UCSC Ensembl
Outerchr10:8869833..9013986hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38144154
hg19144154
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154550
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004587
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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