A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129293



Internal ID20696333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180580250..180584297hg38UCSC Ensembl
chr5:180007250..180011297hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384048
hg194048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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