A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053018



Internal ID21962252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77129271..77129271hg38UCSC Ensembl
chr1:77594956..77594956hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533398
Samples
Known GenesPIGK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053018
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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