A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060289



Internal ID21969523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7367755..7367903hg38UCSC Ensembl
chr19:7432641..7432789hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060289
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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