A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982912



Internal ID18859543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:122926204..122926283hg38UCSC Ensembl
Outerchr11:122796912..122796991hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138082
Supporting Variants
SamplesKWS1
Known GenesC11orf63
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982912
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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