A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102119



Internal ID20669159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30049287..30050595hg38UCSC Ensembl
chr3:30090778..30092086hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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