A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189536



Internal ID21328382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4863651..4863651hg38UCSC Ensembl
chr10:4905843..4905843hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936587
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189536
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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