A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524880



Internal ID20898241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36612944..36613704hg38UCSC Ensembl
chr19:37103846..37104606hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046583
Samples
Known GenesZNF382
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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