A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524594



Internal ID20897955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43829345..43830852hg38UCSC Ensembl
chr19:44333497..44335004hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381508
hg191508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198834
Samples
Known GenesZNF283
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524594
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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