A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526124



Internal ID20899485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14696789..14722825hg38UCSC Ensembl
chr19:14807601..14833637hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3826037
hg1926037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047190
Samples
Known GenesZNF333
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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