A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102196



Internal ID22011431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50894284..50894284hg38UCSC Ensembl
chr18:48420654..48420654hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622048
Samples
Known GenesME2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102196
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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