A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136113



Internal ID18922195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:23439471..23440071hg38UCSC Ensembl
Outerchr10:23728400..23729000hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989718
SamplesKWS2
Known GenesOTUD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136113
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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