A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335261



Internal ID20868453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31492728..31506032hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3813305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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