A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101059



Internal ID22010292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37337737..37337737hg38UCSC Ensembl
chr19:37828639..37828639hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632411
Samples
Known GenesHKR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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