A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103789



Internal ID22013022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8896256..8896256hg38UCSC Ensembl
chr19:9006932..9006932hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634352
Samples
Known GenesMUC16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103789
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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