A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036726



Internal ID21946069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29692212..29692418hg38UCSC Ensembl
chr13:30266349..30266555hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036726
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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