A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367559



Internal ID22593228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44713185..44864431hg38UCSC Ensembl
chr10:45208633..45359879hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38151247
hg19151247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920671
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367559
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004


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