A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000658



Internal ID21910001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139707310..139707853hg38UCSC Ensembl
chr5:139086895..139087438hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000658
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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