A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934426



Internal ID22709752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44172048..44205002hg38UCSC Ensembl
chr15:44464246..44497200hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3832955
hg1932955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376070
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934426
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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