A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980762



Internal ID18863219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:129375605..129375905hg38UCSC Ensembl
Outerchr11:129245500..129245800hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143553
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980762
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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