A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527271



Internal ID20900632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45870021..45870408hg38UCSC Ensembl
chr19:46373279..46373666hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046536
Samples
Known GenesFOXA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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