A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190428



Internal ID21329279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70239932..70239932hg38UCSC Ensembl
chr10:71999688..71999688hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928042
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190428
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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