A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532685



Internal ID20906046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:772525..1226907hg38UCSC Ensembl
chr18:772526..1226908hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38454383
hg19454383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197231
Samples
Known GenesADCYAP1, YES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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