A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595196



Internal ID6635470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7507741..7629043hg38UCSC Ensembl
chr3:7549428..7670730hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38121303
hg19121303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10916335
SamplesHG01798
Known GenesGRM7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595196
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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