A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001418



Internal ID21910761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73660531..73660806hg38UCSC Ensembl
chr6:74370254..74370529hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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