A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068849



Internal ID21978082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60520103..60520103hg38UCSC Ensembl
chr5:59815930..59815930hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382128
hg192128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556639
Samples
Known GenesPART1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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