A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980889



Internal ID18868365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72781455..72782055hg38UCSC Ensembl
Outerchr11:72492500..72493100hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118220
Supporting Variants
SamplesKWS1
Known GenesSTARD10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980889
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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