A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132228



Internal ID20699268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74303801..74309600hg38UCSC Ensembl
chr5:73599626..73605425hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409827
Supporting Variants
Samples
Known GenesLOC102503429
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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