A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017647



Internal ID20584687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30303961..30304416hg38UCSC Ensembl
chr14:30773167..30773622hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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