A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867903



Internal ID22642838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32435591..32440203hg38UCSC Ensembl
chr17:30762609..30767221hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg384613
hg194613
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867903
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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