A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006073



Internal ID22067704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89183210..89191098hg38UCSC Ensembl
Outerchr10:89178916..89194672hg38UCSC Ensembl
Innerchr10:90942967..90950855hg19UCSC Ensembl
Outerchr10:90938673..90954429hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3815757
hg1915757
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154645
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006073
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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