A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490377



Internal ID22548300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184099436..184101418hg38UCSC Ensembl
chr3:183817224..183819206hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381983
hg191983
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835693
Supporting Variants
Samples
Known GenesHTR3E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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