A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025546



Internal ID21934889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29641699..29647707hg38UCSC Ensembl
chr13:30215836..30221844hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg386009
hg196009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025546
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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