A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374779



Internal ID22600448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48598769..48599554hg38UCSC Ensembl
chr14:49067972..49068757hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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