A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531592



Internal ID20904953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58263870..58269909hg38UCSC Ensembl
chr18:55931102..55937141hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg386040
hg196040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3381n223
Supporting Variantsnssv18042323
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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