A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159853



Internal ID21427384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113900634..113900634hg38UCSC Ensembl
chr9:116662914..116662914hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637529
Supporting Variants
SamplesHG00731
Known GenesZNF618
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159853
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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