A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517687



Internal ID20891048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13148653..13149379hg38UCSC Ensembl
chr19:13259467..13260193hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045402
Samples
Known GenesSTX10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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