A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531591



Internal ID20904952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52328888..52338555hg38UCSC Ensembl
chr19:52832141..52841808hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg389668
hg199668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048778
Samples
Known GenesZNF610
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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