A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517477



Internal ID20890838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4135932..4137068hg38UCSC Ensembl
chr18:4135932..4137068hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041754
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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