A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438178



Internal ID22496048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10679719..10679774hg38UCSC Ensembl
chr8:10537229..10537284hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925994
Supporting Variants
Samples
Known GenesC8orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438178
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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