A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154657



Internal ID22085162
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004527, nssv4004528
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154657
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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