A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929611



Internal ID22704867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35410403..35410706hg38UCSC Ensembl
chr14:35879609..35879912hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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