A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050096



Internal ID21959329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34923092..34924323hg38UCSC Ensembl
chr19:35413996..35415227hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050096
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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