A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529359



Internal ID20902720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34325427..34510321hg38UCSC Ensembl
chr19:34816332..35001226hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38184895
hg19184895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197757
Samples
Known GenesGPI, KIAA0355, PDCD2L, UBA2, WTIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529359
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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