A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984371



Internal ID19211230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32740275..32741590hg38UCSC Ensembl
Outerchr3:32781767..32783082hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121728
Supporting Variants
SamplesKWS1
Known GenesCNOT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984371
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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