A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013569



Internal ID21922912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94658852..94658964hg38UCSC Ensembl
chr5:93994557..93994669hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554859
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013569
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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