A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351759



Internal ID22577428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128127443..128138586hg38UCSC Ensembl
chr10:129925707..129936850hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3811144
hg1911144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351759
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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