A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596353



Internal ID6983670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61803567..61906298hg38UCSC Ensembl
Innerchr3:61803717..61906148hg38UCSC Ensembl
Outerchr3:61803417..61906448hg38UCSC Ensembl
chr3:61789241..61891972hg19UCSC Ensembl
Innerchr3:61789391..61891822hg19UCSC Ensembl
Outerchr3:61789091..61892122hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38102732
hg19102732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv896e214
Supporting Variantsessv11026176
SamplesHG02127
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596353
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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