A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134045



Internal ID18939836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96887871..96887934hg38UCSC Ensembl
Outerchr10:98647628..98647691hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970384
SamplesKWS2
Known GenesLCOR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134045
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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