A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981762



Internal ID18872081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:63863724..63864424hg38UCSC Ensembl
Outerchr3:63849400..63850100hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118973
Supporting Variants
SamplesKWS1
Known GenesTHOC7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981762
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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