A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375011



Internal ID22600680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75317897..75319308hg38UCSC Ensembl
chr14:75784600..75786011hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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