A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528704



Internal ID20902065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38868474..39233265hg38UCSC Ensembl
chr18:36448438..36813229hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38364792
hg19364792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040102
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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