A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006065



Internal ID21915408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164541687..164565906hg38UCSC Ensembl
chr5:163968693..163992912hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3824220
hg1924220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563432
Samples
Known GenesLOC102546299
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006065
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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