A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015628



Internal ID20582668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102137468..102143644hg38UCSC Ensembl
chr14:102603805..102609981hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg386177
hg196177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510690
Supporting Variants
Samples
Known GenesHSP90AA1, WDR20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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