A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143523



Internal ID18927166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:119206688..119207988hg38UCSC Ensembl
Outerchr10:120966200..120967500hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980729
SamplesKWS1
Known GenesGRK5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143523
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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