A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612352



Internal ID6999253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15210337..15284647hg38UCSC Ensembl
chr7:15249962..15324272hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3874311
hg1974311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1271e214
Supporting Variantsessv12686005, essv12686008, essv12686007, essv12686006
SamplesHG01462, HG01632, HG02554, HG02501
Known GenesAGMO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612352
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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