A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144033



Internal ID20711073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52924995..52926811hg38UCSC Ensembl
chr6:52789793..52791609hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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