A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411611



Internal ID21069164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:127172890..127181439hg38UCSC Ensembl
chr5:126508582..126517131hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg388550
hg198550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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