A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759384



Internal ID20535244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138437284..138437284hg38UCSC Ensembl
chr6:138758421..138758421hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261587
Samples
Known GenesNHSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759384
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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