A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029209



Internal ID21938552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58130077..58131207hg38UCSC Ensembl
chr18:55797309..55798439hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637360
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029209
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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