A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062368



Internal ID21971601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75518018..75518018hg38UCSC Ensembl
chr5:74813843..74813843hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551705
Samples
Known GenesPOLK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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