A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612350



Internal ID6999251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15202593..15287925hg38UCSC Ensembl
chr7:15242218..15327550hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3885333
hg1985333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1271e214
Supporting Variantsessv12686002, essv12686003, essv12686001
SamplesHG01462, HG01632, HG02554
Known GenesAGMO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612350
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer