A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015805



Internal ID21925148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6369225..6369298hg38UCSC Ensembl
chr6:6369458..6369531hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563338
Samples
Known GenesLY86-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015805
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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