A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530057



Internal ID20903418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16014385..16030397hg38UCSC Ensembl
chr19:16125195..16141207hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3816013
hg1916013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044459
Samples
Known GenesLINC00661
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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