A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010071



Internal ID21919414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61278230..61386108hg38UCSC Ensembl
chr5:60574057..60681935hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38107879
hg19107879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547175
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010071
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer