A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329074



Internal ID20862225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154113115..154114016hg38UCSC Ensembl
chr1:154085591..154086492hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052012
Samples
Known GenesNUP210L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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