A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006850



Internal ID21916193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180617977..180618215hg38UCSC Ensembl
chr5:180044977..180045215hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562374
Samples
Known GenesFLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006850
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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