A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534319



Internal ID20907680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19152178..19153621hg38UCSC Ensembl
chr19:19262987..19264430hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381444
hg191444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045977
Samples
Known GenesMEF2B, MEF2BNB-MEF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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