A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521086



Internal ID20894447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74566931..74575550hg38UCSC Ensembl
chr18:72234166..72242785hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg388620
hg198620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043916
Samples
Known GenesCNDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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