A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003091



Internal ID18846098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:95981187..95981497hg38UCSC Ensembl
Outerchr13:96633441..96633751hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151668
Supporting Variants
SamplesKWB1
Known GenesUGGT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003091
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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