A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631067



Internal ID7017882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126421201..126510243hg38UCSC Ensembl
chr12:126905747..126994789hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3889043
hg1989043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14626019
SamplesHG03916
Known GenesLOC100128554
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631067
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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