A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485129



Internal ID22543040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137060298..137063440hg38UCSC Ensembl
chr3:136779140..136782282hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383143
hg193143
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485129
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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