A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025519



Internal ID21934862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91213824..91213889hg38UCSC Ensembl
chr13:91866078..91866143hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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