A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005528



Internal ID21914871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41764727..41765977hg38UCSC Ensembl
chr6:41732465..41733715hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005528
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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