A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015663



Internal ID21925006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120096895..120163243hg38UCSC Ensembl
chr6:120418041..120484389hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3866349
hg1966349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015663
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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