A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212501



Internal ID20779541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119001600..119011301hg38UCSC Ensembl
chr5:118337295..118346996hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg389702
hg199702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212501
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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