A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463413



Internal ID22521299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26741328..26743851hg38UCSC Ensembl
chr1:27067819..27070342hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382524
hg192524
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829670
Supporting Variants
Samples
Known GenesARID1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463413
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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