A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521927



Internal ID20895288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4137901..4141200hg38UCSC Ensembl
chr18:4137901..4141200hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041756
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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