A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128706



Internal ID19253920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20429947..20494647hg38UCSC Ensembl
Outerchr15:20635200..20699900hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3864701
hg1964701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960619
SamplesKWS1
Known GenesHERC2P3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128706
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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