A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525423



Internal ID20898784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1612551..1612907hg38UCSC Ensembl
chr19:1612550..1612906hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044466
Samples
Known GenesTCF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525423
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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