A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329752



Internal ID20862905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86407647..86409956hg38UCSC Ensembl
chr1:86873330..86875639hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg382310
hg192310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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