A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612407



Internal ID6999308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16874541..16996126hg38UCSC Ensembl
chr7:16914165..17035750hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38121586
hg19121586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1273e214
Supporting Variantsessv12688318, essv12688316, essv12688317, essv12688319
SamplesHG01779, HG01673, HG01675, HG02455
Known GenesAGR3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612407
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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