A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516598



Internal ID20889959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36192032..36193485hg38UCSC Ensembl
chr19:36682934..36684387hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046336
Samples
Known GenesZNF565
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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