A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485101



Internal ID22543012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135574772..135612259hg38UCSC Ensembl
chr3:135293614..135331101hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3837488
hg1937488
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834671
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485101
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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