A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585951



Internal ID21534499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29145709..29145926hg38UCSC Ensembl
chr12:29298642..29298859hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079370
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585951
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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