A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005446



Internal ID21914789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44107407..44107524hg38UCSC Ensembl
chr6:44075144..44075261hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005446
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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