A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999694



Internal ID19194258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:65920736..65923661hg38UCSC Ensembl
Outerchr15:66213074..66215999hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382926
hg192926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152514
Supporting Variants
SamplesKWB1
Known GenesMEGF11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999694
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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