A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992763



Internal ID19241292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:27188153..27194253hg38UCSC Ensembl
Outerchr15:27433300..27439400hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141258
Supporting Variants
SamplesKWS2
Known GenesGABRG3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992763
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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