A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360886



Internal ID22586555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167913652..167913729hg38UCSC Ensembl
chr1:167882890..167882967hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886479
Supporting Variants
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360886
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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