A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129250



Internal ID20696290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180092221..180098600hg38UCSC Ensembl
chr5:179519221..179525600hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386380
hg196380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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