A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517694



Internal ID20891055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12612999..12613825hg38UCSC Ensembl
chr19:12723813..12724639hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045361
Samples
Known GenesZNF791
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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