A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987182



Internal ID19220784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22472559..22482396hg38UCSC Ensembl
Outerchr15:23390700..23400800hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg389838
hg1910101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132407
Supporting Variants
SamplesKWS1
Known GenesHERC2P7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987182
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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