A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394568



Internal ID22452438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12905428..12910832hg38UCSC Ensembl
chr19:13016242..13021646hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936105
Supporting Variants
Samples
Known GenesSYCE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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