A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994365



Internal ID18865156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:27471753..27473253hg38UCSC Ensembl
Outerchr11:27493300..27494800hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143676
Supporting Variants
SamplesKWS1
Known GenesLGR4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994365
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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