A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317576



Internal ID20850663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83590014..83595966hg38UCSC Ensembl
chr1:84055697..84061649hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385953
hg195953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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