A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035200



Internal ID21944543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61557038..61557660hg38UCSC Ensembl
chr13:62131171..62131793hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035200
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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