A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162955



Internal ID21412310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90550383..90550383hg38UCSC Ensembl
chr9:93312665..93312665hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630247
Supporting Variants
SamplesHG00513
Known GenesLOC340515
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162955
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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