A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615216



Internal ID6655415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139505307..139545353hg38UCSC Ensembl
chr7:139190053..139230099hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3840047
hg1940047
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12982072, essv12982070, essv12982071
SamplesHG02890, HG03382, HG03410
Known GenesCLEC2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615216
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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