A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612249



Internal ID6999150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12332122..12356965hg38UCSC Ensembl
chr7:12371748..12396591hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3824844
hg1924844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12683725, essv12683724
SamplesHG04229, HG01950
Known GenesVWDE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612249
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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