A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144986



Internal ID20712026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50690131..50693027hg38UCSC Ensembl
chr6:50657844..50660740hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382897
hg192897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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