A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929903



Internal ID22705162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37000826..37000876hg38UCSC Ensembl
chr14:37470031..37470081hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373826
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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