A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019031



Internal ID21928374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31617734..31617787hg38UCSC Ensembl
chr10:31906662..31906715hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019031
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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