A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064424



Internal ID21973657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73508422..73508422hg38UCSC Ensembl
chr6:74218145..74218145hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064424
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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