A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107509



Internal ID21401286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:108726419..108727228hg38UCSC Ensembl
chr2:109342875..109343684hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583639
Supporting Variants
SamplesHG00096
Known GenesRANBP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107509
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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