A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613498



Internal ID6653707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66080316..66095812hg38UCSC Ensembl
chr7:65545303..65560799hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3815497
hg1915497
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12816596, essv12816598, essv12816597
SamplesHG02666, NA19209, HG02573
Known GenesASL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613498
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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