A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534559



Internal ID20907920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6386496..6397905hg38UCSC Ensembl
chr19:6386507..6397916hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811410
hg1911410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049654
Samples
Known GenesGTF2F1, MIR6790, MIR6885
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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