A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526723



Internal ID20900084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47424488..47430965hg38UCSC Ensembl
chr19:47927745..47934222hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386478
hg196478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198950
Samples
Known GenesSLC8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526723
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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