A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530470



Internal ID20903831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56505055..56511630hg38UCSC Ensembl
chr19:57016424..57022999hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg386576
hg196576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049331
Samples
Known GenesZNF471
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530470
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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