A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432526



Internal ID22490396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11060827..11073392hg38UCSC Ensembl
chr8:10918337..10930902hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3812566
hg1912566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927341
Supporting Variants
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432526
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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