A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586604



Internal ID21778647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138217570..138217570hg38UCSC Ensembl
chr9:141108020..141108020hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088379
Supporting Variants
Samples
Known GenesFAM157B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586604
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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