A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962610



Internal ID19213008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:69286005..69286090hg38UCSC Ensembl
Outerchr15:69578344..69578429hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129180
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962610
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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