A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977219



Internal ID19247295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:79747358..79750158hg38UCSC Ensembl
Outerchr15:80039700..80042500hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139633
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977219
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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