A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999921



Internal ID19186711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:30355096..30363497hg38UCSC Ensembl
Outerchr15:30647299..30655700hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg388402
hg198402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152738
Supporting Variants
SamplesKWB1
Known GenesCHRFAM7A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999921
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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