A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637263



Internal ID21585568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113900989..113900989hg38UCSC Ensembl
chr9:116663269..116663269hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159857
SamplesHG00731
Known GenesZNF618
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637263
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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