A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885027



Internal ID22660011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50678418..50679618hg38UCSC Ensembl
chr17:48755779..48756979hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475063, nssv17475062
Samples
Known GenesABCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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