A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532946



Internal ID20906307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10664953..10668900hg38UCSC Ensembl
chr19:10775629..10779576hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383948
hg193948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044940
Samples
Known GenesILF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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