A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066028



Internal ID21975261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57184687..57184687hg38UCSC Ensembl
chr5:56480514..56480514hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382604
hg192604
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537805
Samples
Known GenesGPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066028
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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