A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125176



Internal ID19258193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:60897122..60897180hg38UCSC Ensembl
Outerchr10:62656880..62656938hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977981
SamplesKWS2
Known GenesRHOBTB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125176
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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