A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319521



Internal ID20852616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169064816..169067615hg38UCSC Ensembl
chr1:169034054..169036853hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053637
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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