A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370315



Internal ID22595984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55077962..55083666hg38UCSC Ensembl
chr14:55544680..55550384hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg385705
hg195705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370315
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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