A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535492



Internal ID20908853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57662149..57967273hg38UCSC Ensembl
chr19:58173517..58478641hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38305125
hg19305125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199713
Samples
Known GenesC19orf18, FKBP1AP1, ZNF154, ZNF256, ZNF417, ZNF418, ZNF551, ZNF552, ZNF586, ZNF587, ZNF587B, ZNF671, ZNF776, ZNF814, ZSCAN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535492
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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