A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988096



Internal ID19210514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:37982488..37982542hg38UCSC Ensembl
Outerchr15:38274689..38274743hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133215
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988096
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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