A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363791



Internal ID22589460
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 StatusS
Merged Variantsnsv5868779
Supporting Variants
Samples
Known GenesLINC00303
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363791
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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