A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098299



Internal ID22007532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51635796..51635796hg38UCSC Ensembl
chr17:49713157..49713157hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg384331
hg194331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636243
Samples
Known GenesCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098299
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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