A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013888



Internal ID21923231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63390610..63390674hg38UCSC Ensembl
chr6:64100515..64100579hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013888
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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