A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625685



Internal ID21573990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113900985..113900985hg38UCSC Ensembl
chr9:116663265..116663265hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159856
SamplesHG03486
Known GenesZNF618
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625685
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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