A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328785



Internal ID20861935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199666382..199666783hg38UCSC Ensembl
chr1:199635510..199635911hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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