A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761188



Internal ID22095605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132519151..132519151hg38UCSC Ensembl
chr9:135394538..135394538hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448206
Supporting Variants
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761188
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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