A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378842



Internal ID22436712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95338865..95338924hg38UCSC Ensembl
chr14:95805202..95805261hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378842
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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