A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485069



Internal ID22542980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133014985..133061202hg38UCSC Ensembl
chr3:132733829..132780046hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3846218
hg1946218
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834319
Supporting Variants
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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