A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033035



Internal ID21942378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90495882..90495982hg38UCSC Ensembl
chr13:91148136..91148236hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033035
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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