A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062143



Internal ID21971376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112374770..112374770hg38UCSC Ensembl
chr4:113295926..113295926hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545166
Samples
Known GenesALPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062143
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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