A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4017810



Internal ID22079441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103226498..103232318hg38UCSC Ensembl
Outerchr3:103219973..103244137hg38UCSC Ensembl
Innerchr3:102945342..102951162hg19UCSC Ensembl
Outerchr3:102938817..102962981hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3824165
hg1924165
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156007
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4017810
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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