A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611764



Internal ID6651981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:244861..405949hg38UCSC Ensembl
chr7:284827..445915hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38161089
hg19161089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657180, essv12657181
SamplesHG01797, NA19661
Known GenesFAM20C, LOC100288524, LOC442497
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611764
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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