A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531696



Internal ID20905057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53396844..53470433hg38UCSC Ensembl
chr19:53900097..53973687hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3873590
hg1973591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200179
Samples
Known GenesTPM3P9, ZNF761, ZNF765, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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