A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333418



Internal ID20866594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171673207..171677583hg38UCSC Ensembl
chr1:171642347..171646723hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg384377
hg194377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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