A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595197



Internal ID6635471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7509066..7752803hg38UCSC Ensembl
chr3:7550753..7794490hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38243738
hg19243738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10916337, essv10916336
SamplesHG01798, NA19080
Known GenesGRM7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595197
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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