A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522836



Internal ID20896197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12105601..12108100hg38UCSC Ensembl
chr18:12105600..12108099hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3283n223
Supporting Variantsnssv18038764
Samples
Known GenesANKRD62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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