A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987104



Internal ID19219182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38658969..38699369hg38UCSC Ensembl
Outerchr10:38952100..38992500hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3840401
hg1940401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132332
Supporting Variants
SamplesKWS1
Known GenesACTR3BP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987104
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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