A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099352



Internal ID22008585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44668355..44668355hg38UCSC Ensembl
chr17:42745723..42745723hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628951
Samples
Known GenesC17orf104
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099352
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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