A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527351



Internal ID20900712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48287408..48294344hg38UCSC Ensembl
chr19:48790665..48797601hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg386937
hg196937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048373
Samples
Known GenesZNF114
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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