A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528476



Internal ID20901837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51365161..51431917hg38UCSC Ensembl
chr18:48891531..48958287hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3866757
hg1966757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184402
Samples
Known GenesLOC100287225
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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