A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333738



Internal ID20866918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180859746..180860322hg38UCSC Ensembl
chr1:180828882..180829458hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054607
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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