A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601792



Internal ID6988828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111961515..111973822hg38UCSC Ensembl
Innerchr4:111961565..111973772hg38UCSC Ensembl
Outerchr4:111961415..111973922hg38UCSC Ensembl
chr4:112882671..112894978hg19UCSC Ensembl
Innerchr4:112882721..112894928hg19UCSC Ensembl
Outerchr4:112882571..112895078hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3812308
hg1912308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11565195, essv11565196
SamplesNA20753, HG00119
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601792
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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