A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019068



Internal ID21928411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49486187..49518348hg38UCSC Ensembl
chr10:50694233..50726394hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3832162
hg1932162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585579
Samples
Known GenesERCC6, ERCC6-PGBD3, PGBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019068
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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