A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359020



Internal ID22584689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17567652..17584339hg38UCSC Ensembl
chr10:17609651..17626338hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3816688
hg1916688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359020
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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