A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762962



Internal ID19313888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19796646..19808147hg38UCSC Ensembl
chr15:20001899..20013400hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3811502
hg1911502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075464
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762962
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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