A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529295



Internal ID20902656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17928939..17929693hg38UCSC Ensembl
chr19:18039748..18040502hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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