A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977216



Internal ID19235570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44359902..44364702hg38UCSC Ensembl
Outerchr15:44652100..44656900hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139630
Supporting Variants
SamplesKWS2
Known GenesCASC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977216
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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