A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530933



Internal ID20904294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59498122..59544256hg38UCSC Ensembl
chr18:57165354..57211488hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3846135
hg1946135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196634
Samples
Known GenesCCBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530933
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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