A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868288



Internal ID22643223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45604941..45621282hg38UCSC Ensembl
chr17:43682307..43698648hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3816342
hg1916342
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474415
Samples
Known GenesCRHR1, MGC57346
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868288
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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