A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124032



Internal ID20691073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109761001..109766200hg38UCSC Ensembl
chr5:109096702..109101901hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402715
Supporting Variants
Samples
Known GenesMAN2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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