A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517653



Internal ID20891014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33216621..33218815hg38UCSC Ensembl
chr19:33707527..33709721hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382195
hg192195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197326
Samples
Known GenesSLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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