A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533864



Internal ID20907225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57367860..57368551hg38UCSC Ensembl
chr19:57879228..57879919hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048601
Samples
Known GenesZNF547
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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