A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962335



Internal ID19214424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24892502..24892593hg38UCSC Ensembl
Outerchr15:25137649..25137740hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111113
Supporting Variants
SamplesKWS1
Known GenesSNRPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962335
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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