A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531730



Internal ID20905091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27103395..27230456hg38UCSC Ensembl
chr18:24683359..24810420hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38127062
hg19127062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195985
Samples
Known GenesCHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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