A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161953



Internal ID21450616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33571620..33571620hg38UCSC Ensembl
chr9:33571618..33571618hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631489
Supporting Variants
SamplesHG01505
Known GenesANKRD18B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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