A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960640



Internal ID19208975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76258459..76262559hg38UCSC Ensembl
Outerchr15:76550800..76554900hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128727
Supporting Variants
SamplesKWS1
Known GenesETFA, TYRO3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960640
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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