A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133318



Internal ID20700358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69135006..69141526hg38UCSC Ensembl
chr5:68430833..68437353hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133318
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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