A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533077



Internal ID20906438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58130621..58141889hg38UCSC Ensembl
chr18:55797853..55809121hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3811269
hg1911269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042310
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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