A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611772



Internal ID6651989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:305406..384519hg38UCSC Ensembl
chr7:345372..424485hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3879114
hg1979114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657595, essv12657592, essv12657593, essv12657594
SamplesHG00129, HG01797, NA20126, NA06985
Known GenesLOC442497
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611772
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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