A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017554



Internal ID21926897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177560217..177560273hg38UCSC Ensembl
chr5:176987218..176987274hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017554
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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