A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190415



Internal ID21329247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67849297..67849297hg38UCSC Ensembl
chr10:69609055..69609055hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931463
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190415
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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