A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614427



Internal ID6654633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105529416..105544030hg38UCSC Ensembl
chr7:105169863..105184477hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3814615
hg1914615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913831, essv12913830
SamplesHG02049, HG02017
Known GenesRINT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614427
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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