A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934035



Internal ID22709354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77045365..77045451hg38UCSC Ensembl
chr18:74757321..74757407hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398428
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934035
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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