A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332985



Internal ID20866160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203406693..203409589hg38UCSC Ensembl
chr1:203375821..203378717hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382897
hg192897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer