A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900995



Internal ID22676143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121576470..121731551hg38UCSC Ensembl
chr5:120912165..121067246hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38155082
hg19155082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900995
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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