A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017672



Internal ID20584712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30605845..30606474hg38UCSC Ensembl
chr14:31075051..31075680hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479724
Supporting Variants
Samples
Known GenesG2E3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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