A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518953



Internal ID20892314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76664424..76847645hg38UCSC Ensembl
chr18:74376381..74559601hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38183222
hg19183221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197216
Samples
Known GenesLOC100131655, ZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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