A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128682



Internal ID20695722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150967679..150970847hg38UCSC Ensembl
chr5:150347241..150350409hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383169
hg193169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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