A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533764



Internal ID20907125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13912445..13922665hg38UCSC Ensembl
chr18:13912444..13922664hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3810221
hg1910221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194281
Samples
Known GenesMC2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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