A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622265



Internal ID7009124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7038300..7084697hg38UCSC Ensembl
chr10:7080262..7126659hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3846398
hg1946398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13689283, essv13689282
SamplesHG02497, NA18517
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622265
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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