A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000967



Internal ID21910310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149655477..149655619hg38UCSC Ensembl
chr5:149035040..149035182hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000967
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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