A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523574



Internal ID20896935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34717011..34732989hg38UCSC Ensembl
chr18:32296975..32312953hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3815979
hg1915979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041657
Samples
Known GenesDTNA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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