A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152838



Internal ID19200556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98265372..98265709hg38UCSC Ensembl
Outerchr10:100025129..100025466hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997871
SamplesKWB1
Known GenesLOXL4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152838
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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