A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517524



Internal ID20890885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58229720..58232866hg38UCSC Ensembl
chr18:55896952..55900098hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg383147
hg193147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042318
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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