A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879763



Internal ID22654735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42853445..42869919hg38UCSC Ensembl
chr17:41005462..41021936hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3816475
hg1916475
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473811, nssv17473812
Samples
Known GenesAOC3, AOC4P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879763
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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