A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989163



Internal ID19244300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:148849005..148849323hg38UCSC Ensembl
Outerchr3:148566792..148567110hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121268
Supporting Variants
SamplesKWS2
Known GenesCPB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989163
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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