A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330840



Internal ID20863998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:237924531..237929725hg38UCSC Ensembl
chr1:238087831..238093025hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg385195
hg195195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059255
Samples
Known GenesLOC100130331
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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