A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659145



Internal ID21607450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108850259..108850259hg38UCSC Ensembl
chr12:109244035..109244035hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076760
SamplesNA19238
Known GenesSSH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659145
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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