A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354128



Internal ID22579797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130456989..130475716hg38UCSC Ensembl
chr10:132255253..132273980hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3818728
hg1918728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918310
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354128
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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