A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114838



Internal ID19286241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:69121905..69122018hg38UCSC Ensembl
Outerchr6:69831797..69831910hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975120
SamplesKWS2
Known GenesBAI3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114838
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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