A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527489



Internal ID20900850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58291036..58431327hg38UCSC Ensembl
chr18:55958268..56098559hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38140292
hg19140292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189404
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527489
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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