A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019281



Internal ID21928624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43439619..43439986hg38UCSC Ensembl
chr6:43407357..43407724hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571591
Samples
Known GenesABCC10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019281
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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