A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873258



Internal ID22648203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31591711..31602010hg38UCSC Ensembl
chr17:29918730..29929029hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873258
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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