A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321087



Internal ID20854189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22542180..22544540hg38UCSC Ensembl
chr1:22868673..22871033hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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