A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388997



Internal ID22446867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37162402..37302021hg38UCSC Ensembl
chr14:37631607..37771226hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38139620
hg19139620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937371
Supporting Variants
Samples
Known GenesMIPOL1, SLC25A21, SLC25A21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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