A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531240



Internal ID20904601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45400965..45401430hg38UCSC Ensembl
chr18:42980930..42981395hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041235
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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