A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878499



Internal ID22653464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206866197..206870667hg38UCSC Ensembl
chr1:207039542..207044012hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384471
hg194471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369158
Samples
Known GenesIL20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878499
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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