A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002809



Internal ID21912152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74119022..74119077hg38UCSC Ensembl
chr5:73414847..73414902hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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