A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321999



Internal ID20855108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83526076..83526605hg38UCSC Ensembl
chr1:83991759..83992288hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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