A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016739



Internal ID20583779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23544752..23552762hg38UCSC Ensembl
chr14:24013961..24021971hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg388011
hg198011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477433
Supporting Variants
Samples
Known GenesTHTPA, ZFHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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