A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136696



Internal ID20703736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98576301..98577300hg38UCSC Ensembl
chr5:97912005..97913004hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410797
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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