A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989002



Internal ID19238521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102601115..102601431hg38UCSC Ensembl
Outerchr11:102471846..102472162hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135443
Supporting Variants
SamplesKWS2
Known GenesMMP20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989002
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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