A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367142



Internal ID22592811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111414892..111414960hg38UCSC Ensembl
chr1:111957514..111957582hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885089
Supporting Variants
Samples
Known GenesOVGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367142
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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