A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076505



Internal ID21985738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165122252..165122252hg38UCSC Ensembl
chr6:165535741..165535741hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076505
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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