A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527655



Internal ID20901016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67588192..68015024hg38UCSC Ensembl
chr18:65255429..65682261hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38426833
hg19426833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197594
Samples
Known GenesLOC643542
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527655
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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