A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999837



Internal ID19193039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:100912892..100913179hg38UCSC Ensembl
Outerchr15:101453097..101453384hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152655
Supporting Variants
SamplesKWB1
Known GenesALDH1A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999837
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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