A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980879



Internal ID19210992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:46121549..46122049hg38UCSC Ensembl
Outerchr11:46143100..46143600hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118210
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980879
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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