A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990627



Internal ID18883343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:124960242..124960350hg38UCSC Ensembl
Outerchr11:124830138..124830246hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138084
Supporting Variants
SamplesKWS2
Known GenesCCDC15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990627
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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