A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004528



Internal ID22066159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113448998..113457106hg38UCSC Ensembl
Outerchr10:113444969..113459555hg38UCSC Ensembl
Innerchr10:115208757..115216865hg19UCSC Ensembl
Outerchr10:115204728..115219314hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3814587
hg1914587
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154657
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004528
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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