A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128492



Internal ID20695532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17342701..17354300hg38UCSC Ensembl
chr5:17342810..17354409hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0028


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