A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970495



Internal ID18893335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68755878..68755933hg38UCSC Ensembl
Outerchr11:68523346..68523401hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134152
Supporting Variants
SamplesKWS2
Known GenesCPT1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970495
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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