A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149576



Internal ID19200580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21155868..21158050hg38UCSC Ensembl
Outerchr13:21730007..21732189hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382183
hg192183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000877
SamplesKWB1
Known GenesSKA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149576
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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