A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961875



Internal ID19219747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68132430..68161885hg38UCSC Ensembl
Outerchr15:68424768..68454223hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3829456
hg1929456
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120310
Supporting Variants
SamplesKWS1
Known GenesPIAS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961875
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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