A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612922



Internal ID6999821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40137547..40160173hg38UCSC Ensembl
chr7:40177146..40199772hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3822627
hg1922627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12750053, essv12750054, essv12750052, essv12750051
SamplesNA18592, HG00457, HG00245, NA18553
Known GenesC7orf10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612922
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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