A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029269



Internal ID21938612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58129985..58130082hg38UCSC Ensembl
chr18:55797217..55797314hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632084
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029269
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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