A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11540536



Internal ID4935072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96807867..96815406hg38UCSC Ensembl
Innerchr4:96807867..96815406hg38UCSC Ensembl
Outerchr4:96807639..96815591hg38UCSC Ensembl
chr4:97729018..97736557hg19UCSC Ensembl
Innerchr4:97729018..97736557hg19UCSC Ensembl
Outerchr4:97728790..97736742hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg387540
hg197540
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601498
Supporting Variants
SamplesNA12776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11540536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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