A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534613



Internal ID20907974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10066696..10075103hg38UCSC Ensembl
chr19:10177372..10185779hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388408
hg198408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044271
Samples
Known GenesC3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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