A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058733



Internal ID21967966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37751554..37751641hg38UCSC Ensembl
chr19:38242194..38242281hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630279
Samples
Known GenesZNF573
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058733
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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