A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518621



Internal ID20891982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37363982..37385410hg38UCSC Ensembl
chr19:37854884..37876312hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3821429
hg1921429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198080
Samples
Known GenesHKR1, ZNF527
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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