A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529175



Internal ID20902536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40636135..40637084hg38UCSC Ensembl
chr19:41142040..41142989hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529175
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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