A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038791



Internal ID21948134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73574852..73574904hg38UCSC Ensembl
chr13:74148989..74149041hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038791
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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