A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129756



Internal ID20696796
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 StatusS
Merged Variantsnsv6375945
Supporting Variants
Samples
Known GenesLINC01019
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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