A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132332



Internal ID19262064
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 StatusM
Merged Variants
Supporting Variantsnssv3987104
SamplesKWS1
Known GenesACTR3BP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132332
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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