A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328126



Internal ID20861271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87488151..87503742hg38UCSC Ensembl
chr1:87953834..87969425hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3815592
hg1915592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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