A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868779



Internal ID22643714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204034854..204035616hg38UCSC Ensembl
chr1:204003982..204004744hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363791
Samples
Known GenesLINC00303
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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