A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875561



Internal ID22650519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75408832..75411928hg38UCSC Ensembl
chr17:73404913..73408009hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383097
hg193097
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875561
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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