A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877599



Internal ID22652564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42616591..42631928hg38UCSC Ensembl
chr17:40768609..40783946hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3815338
hg1915338
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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