A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054631



Internal ID21963864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12758709..12760078hg38UCSC Ensembl
chr19:12869523..12870892hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054631
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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