A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529054



Internal ID20902415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36115909..36119810hg38UCSC Ensembl
chr18:33695872..33699773hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039746
Samples
Known GenesSLC39A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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