A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189247



Internal ID21328093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63740044..63740044hg38UCSC Ensembl
chr3:63725720..63725720hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927865
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189247
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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