A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056924



Internal ID21966160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34354517..34358197hg38UCSC Ensembl
chr19:34845422..34849102hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383681
hg193681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628308
Samples
Known GenesKIAA0355
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056924
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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