A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136241



Internal ID20703281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98750021..98752692hg38UCSC Ensembl
chr5:98085725..98088396hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382672
hg192672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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