A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937907



Internal ID22713281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100585243..100585418hg38UCSC Ensembl
chr14:101051580..101051755hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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