A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143525



Internal ID18923021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132186696..132187096hg38UCSC Ensembl
Outerchr10:134000200..134000600hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980732
SamplesKWS1
Known GenesDPYSL4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143525
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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