A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034944



Internal ID21944287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36671764..36672638hg38UCSC Ensembl
chr13:37245901..37246775hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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