A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009869



Internal ID21919212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34662002..34662181hg38UCSC Ensembl
chr6:34629779..34629958hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560143
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009869
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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