A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128657



Internal ID20695697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150590763..150592127hg38UCSC Ensembl
chr5:149970325..149971689hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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