A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898756



Internal ID22673877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57325185..57325295hg38UCSC Ensembl
chr5:56621012..56621122hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898756
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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