A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128692



Internal ID20695732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151235404..151237322hg38UCSC Ensembl
chr5:150614965..150616883hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381919
hg191919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402098
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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