A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014618



Internal ID21923961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14818780..14820359hg38UCSC Ensembl
chr6:14819011..14820590hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014618
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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