A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917513



Internal ID22692732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61458185..61458257hg38UCSC Ensembl
chr10:63217943..63218015hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917513
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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