A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009112



Internal ID21918455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75727973..75728079hg38UCSC Ensembl
chr6:76437689..76437795hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009112
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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