A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602907



Internal ID21551567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66362372..66363208hg38UCSC Ensembl
chr12:66756152..66756988hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093241
SamplesHG03486
Known GenesGRIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602907
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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