A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615013



Internal ID7001902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130001888..130012159hg38UCSC Ensembl
chr7:129641728..129651999hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3810272
hg1910272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12971758
SamplesHG00103
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615013
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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