A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152323



Internal ID19201200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113624974..113625078hg38UCSC Ensembl
Outerchr13:114279289..114279393hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996930
SamplesKWB1
Known GenesTFDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152323
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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