A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526966



Internal ID20900327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3522201..3525700hg38UCSC Ensembl
chr18:3522199..3525698hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041685
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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