A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315923



Internal ID20848998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211398612..211400940hg38UCSC Ensembl
chr1:211571954..211574282hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg382329
hg192329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057415
Samples
Known GenesLINC00467
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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