A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886479



Internal ID22661466
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 StatusM
Merged Variants
Supporting Variantsnssv17360886
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886479
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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