A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122548



Internal ID18930384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:92599281..92599352hg38UCSC Ensembl
Outerchr10:94359038..94359109hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970757
SamplesKWS2
Known GenesKIF11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122548
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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