A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375945



Internal ID21033498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3506692..3507274hg38UCSC Ensembl
chr5:3506806..3507388hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129756
Samples
Known GenesLINC01019
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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