A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351257



Internal ID22576926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2156520..2156617hg38UCSC Ensembl
chr10:2198714..2198811hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351257
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.065


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