A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012756



Internal ID21922099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138108328..138108543hg38UCSC Ensembl
chr5:137444017..137444232hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012756
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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