A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960633



Internal ID19207624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22517196..22542596hg38UCSC Ensembl
Outerchr15:23330500..23355900hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3825401
hg1925401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128720
Supporting Variants
SamplesKWS1
Known GenesHERC2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960633
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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