A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528683



Internal ID20902044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57399116..57399492hg38UCSC Ensembl
chr19:57910484..57910860hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048607
Samples
Known GenesZNF548
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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