A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524963



Internal ID20898324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17494324..17495810hg38UCSC Ensembl
chr19:17605133..17606619hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381487
hg191487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045018
Samples
Known GenesSLC27A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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