A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611796



Internal ID6998699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:904223..922273hg38UCSC Ensembl
chr7:943860..961909hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3818051
hg1918050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12662080
SamplesHG00705
Known GenesADAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611796
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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