A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004444



Internal ID21913787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74468616..74474133hg38UCSC Ensembl
chr6:75178332..75183849hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385518
hg195518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004444
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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