A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614426



Internal ID7001320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105522085..105536025hg38UCSC Ensembl
chr7:105162532..105176472hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3813941
hg1913941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913828, essv12913829
SamplesHG02017, HG02049
Known GenesPUS7, RINT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614426
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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