A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075509



Internal ID21984742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2515036..2515036hg38UCSC Ensembl
chr7:2554670..2554670hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568591
Samples
Known GenesLFNG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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