A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129131



Internal ID20696171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24811271..24819891hg38UCSC Ensembl
chr5:24811380..24820000hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg388621
hg198621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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