A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528037



Internal ID20901398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58129701..58130281hg38UCSC Ensembl
chr18:55796933..55797513hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184117
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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