A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353705



Internal ID22579374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23420963..23422732hg38UCSC Ensembl
chr10:23709892..23711661hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg381770
hg191770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353705
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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