A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154546



Internal ID22085051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4656097..4677604hg38UCSC Ensembl
Outerchr10:4655386..4678434hg38UCSC Ensembl
Innerchr10:4698289..4719796hg19UCSC Ensembl
Outerchr10:4697578..4720626hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3823049
hg1923049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004582
Samples
Known GenesLINC00704, LINC00705
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154546
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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