A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121535



Internal ID19254933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9923268..9923366hg38UCSC Ensembl
Outerchr18:9923265..9923363hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965538
SamplesKWS2
Known GenesVAPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121535
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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