A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527590



Internal ID20900951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12557623..12559475hg38UCSC Ensembl
chr18:12557622..12559474hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381853
hg191853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039406
Samples
Known GenesSPIRE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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