A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332390



Internal ID20865561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109607801..109609800hg38UCSC Ensembl
chr1:110150423..110152422hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050822
Samples
Known GenesGNAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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