A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11558187



Internal ID1016097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108685974..108687728hg38UCSC Ensembl
Innerchr4:108686012..108687691hg38UCSC Ensembl
Outerchr4:108685937..108687766hg38UCSC Ensembl
chr4:109607130..109608884hg19UCSC Ensembl
Innerchr4:109607168..109608847hg19UCSC Ensembl
Outerchr4:109607093..109608922hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601726
Supporting Variants
SamplesHG00637
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11558187
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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