A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517662



Internal ID20891023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45051352..45087289hg38UCSC Ensembl
chr19:45554610..45590547hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3835938
hg1935938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198864
Samples
Known GenesCLASRP, GEMIN7, ZNF296
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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