A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034638



Internal ID21943981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94950948..94951334hg38UCSC Ensembl
chr13:95603202..95603588hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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