A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634341



Internal ID21582646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36645304..36645304hg38UCSC Ensembl
chr9:36645301..36645301hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161752
SamplesHG00512
Known GenesMELK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634341
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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