A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014361



Internal ID21923704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168524930..168524986hg38UCSC Ensembl
chr5:167951935..167951991hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014361
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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