A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520972



Internal ID20894333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10886647..10900165hg38UCSC Ensembl
chr19:10997323..11010841hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813519
hg1913519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044951
Samples
Known GenesCARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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