A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021910



Internal ID21931253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32000360..32000586hg38UCSC Ensembl
chr13:32574497..32574723hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021910
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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