A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973146



Internal ID18879698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:98796256..98796319hg38UCSC Ensembl
Outerchr3:98515100..98515163hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136755
Supporting Variants
SamplesKWS2
Known GenesDCBLD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973146
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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