A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527532



Internal ID20900893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9809071..9809266hg38UCSC Ensembl
chr18:9809068..9809263hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198006
Samples
Known GenesRAB31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527532
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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