A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353932



Internal ID22579601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15597598..15597652hg38UCSC Ensembl
chr10:15639597..15639651hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911744
Supporting Variants
Samples
Known GenesITGA8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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