A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933431



Internal ID22708744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43785002..43785317hg38UCSC Ensembl
chr15:44077200..44077515hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385395
Samples
Known GenesSERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933431
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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