A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878012



Internal ID22652978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48561965..48563320hg38UCSC Ensembl
chr17:46639327..46640682hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381356
hg191356
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474508, nssv17474509
Samples
Known GenesHOXB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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