A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011509



Internal ID21920852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81886660..81887002hg38UCSC Ensembl
chr5:81182479..81182821hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011509
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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