A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935292



Internal ID22710631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70679026..70696992hg38UCSC Ensembl
chr14:71145743..71163709hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3817967
hg1917967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935292
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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