A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614939



Internal ID7001829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126717175..126727819hg38UCSC Ensembl
chr7:126357229..126367873hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3810645
hg1910645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12958284
SamplesHG01360
Known GenesGRM8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614939
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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