A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614108



Internal ID7001003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90555211..90593444hg38UCSC Ensembl
chr7:90184525..90222758hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3838234
hg1938234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12886580, essv12886574, essv12886575, essv12886577, essv12886576, essv12886579, essv12886571, essv12886578, essv12886570, essv12886573, essv12886581, essv12886572, essv12886569
SamplesNA18997, HG00626, HG00452, NA19076, HG01813, NA18966, HG02178, NA18991, HG00584, HG00708, HG00445, HG00580, NA18609
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614108
Frequency
Sample Size2504
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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