A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6511751



Internal ID9847313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121769860..121771645hg38UCSC Ensembl
Outerchr4:121769816..121771695hg38UCSC Ensembl
Innerchr4:122691015..122692800hg19UCSC Ensembl
Outerchr4:122690971..122692850hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381880
hg191880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669490
Supporting Variants
SamplesNA20513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6511751
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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