A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983156



Internal ID18866572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:43320216..43320293hg38UCSC Ensembl
Outerchr11:43341766..43341843hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145518
Supporting Variants
SamplesKWS1
Known GenesAPI5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983156
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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