A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531024



Internal ID20904385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:770417..1453129hg38UCSC Ensembl
chr18:770418..1453130hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38682713
hg19682713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197229
Samples
Known GenesADCYAP1, LINC00470, YES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531024
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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