A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140860



Internal ID20707900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28138248..28140461hg38UCSC Ensembl
chr6:28106026..28108239hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382214
hg192214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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