A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331488



Internal ID20864652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225983499..225994117hg38UCSC Ensembl
chr1:226171200..226181818hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3810619
hg1910619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058394
Samples
Known GenesSDE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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