A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201129



Internal ID21339933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16950603..16950603hg38UCSC Ensembl
chr6:16950834..16950834hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939222
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201129
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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