A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315658



Internal ID20848730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157818454..157836162hg38UCSC Ensembl
chr1:157788244..157805952hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3817709
hg1917709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052717
Samples
Known GenesCD5L, FCRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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