A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534027



Internal ID20907388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58262801..58269900hg38UCSC Ensembl
chr18:55930033..55937132hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3381n223
Supporting Variantsnssv18042321
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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