A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228306



Internal ID22370536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25803224..25803819hg38UCSC Ensembl
chr12:25956158..25956753hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361662
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228306
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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