A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611948



Internal ID6998850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4728165..4731377hg38UCSC Ensembl
Innerchr7:4728165..4731377hg38UCSC Ensembl
Outerchr7:4727999..4731529hg38UCSC Ensembl
chr7:4767796..4771008hg19UCSC Ensembl
Innerchr7:4767796..4771008hg19UCSC Ensembl
Outerchr7:4767630..4771160hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12671522
SamplesHG02373
Known GenesFOXK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611948
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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