A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526868



Internal ID20900229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11630884..11659326hg38UCSC Ensembl
chr18:11630883..11659325hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3828443
hg1928443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187700
Samples
Known GenesMIR7153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526868
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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