A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977986



Internal ID22752921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50216611..50216611hg38UCSC Ensembl
chr15:50508808..50508808hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380619
Samples
Known GenesSLC27A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977986
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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