A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596331



Internal ID6983648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61087272..61128557hg38UCSC Ensembl
chr3:61072945..61114230hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3841286
hg1941286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11025987
SamplesNA20847
Known GenesFHIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596331
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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