A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525335



Internal ID20898696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:317246..317567hg38UCSC Ensembl
chr19:317246..317567hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047614
Samples
Known GenesMIER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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