A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989731



Internal ID18900008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14292654..14296854hg38UCSC Ensembl
Outerchr11:14314200..14318400hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136125
Supporting Variants
SamplesKWS2
Known GenesRRAS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989731
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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