A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334868



Internal ID20868057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167611326..167613960hg38UCSC Ensembl
chr1:167580563..167583197hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382635
hg192635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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