A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019929



Internal ID21929272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83263753..83263810hg38UCSC Ensembl
chr6:83973472..83973529hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574241
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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