A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534515



Internal ID20907876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32151901..32231000hg38UCSC Ensembl
chr18:29731864..29810963hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3879100
hg1979100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039956
Samples
Known GenesMEP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534515
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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