A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149745



Internal ID19196028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110907137..110907297hg38UCSC Ensembl
Outerchr13:111559484..111559644hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001047
SamplesKWB1
Known GenesANKRD10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149745
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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