A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481833



Internal ID22539738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85906222..85921254hg38UCSC Ensembl
chr1:86371905..86386937hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3815033
hg1915033
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830515
Supporting Variants
Samples
Known GenesCOL24A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481833
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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