A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611786



Internal ID6652003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:782212..795376hg38UCSC Ensembl
Innerchr7:782212..795376hg38UCSC Ensembl
Outerchr7:781712..795876hg38UCSC Ensembl
chr7:821849..835013hg19UCSC Ensembl
Innerchr7:821849..835013hg19UCSC Ensembl
Outerchr7:821349..835513hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3813165
hg1913165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657949
SamplesNA19149
Known GenesHEATR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611786
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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