A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332198



Internal ID20865367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96487131..96489961hg38UCSC Ensembl
chr1:96952687..96955517hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382831
hg192831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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