A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869757



Internal ID22644692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12773748..12774847hg38UCSC Ensembl
chr17:12677065..12678164hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475418
Samples
Known GenesLOC100128006
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869757
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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