A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521808



Internal ID20895169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10324631..10325594hg38UCSC Ensembl
chr19:10435307..10436270hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044294
Samples
Known GenesRAVER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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