A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982838



Internal ID19221741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:28979035..28991341hg38UCSC Ensembl
Outerchr11:29000582..29012888hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3812307
hg1912307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135430
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982838
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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