A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417773



Internal ID196962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167913656..167913730hg38UCSC Ensembl
chr1:167882894..167882968hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892097
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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