A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075513



Internal ID21984746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50708298..50708298hg38UCSC Ensembl
chr6:50676011..50676011hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075513
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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