A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485202



Internal ID22543113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142566750..142573121hg38UCSC Ensembl
chr3:142285592..142291963hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386372
hg196372
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834948
Supporting Variants
Samples
Known GenesATR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485202
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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