A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030367



Internal ID87955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16143682..16158371hg38UCSC Ensembl
chr10:16185681..16200370hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3814690
hg1914690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030367
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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