A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882892



Internal ID22657869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81004071..81015667hg38UCSC Ensembl
chr17:78977871..78989467hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811597
hg1911597
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882892
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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