A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019808



Internal ID21929151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6640172..6641626hg38UCSC Ensembl
chr6:6640405..6641859hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381455
hg191455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570901
Samples
Known GenesLY86
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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