A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665445



Internal ID9931550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119411947..119430868hg38UCSC Ensembl
Outerchr4:119411790..119431021hg38UCSC Ensembl
Innerchr4:120333102..120352023hg19UCSC Ensembl
Outerchr4:120332945..120352176hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3819232
hg1919232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6057802, essv6043570, essv6552136, essv5505014, essv6169096, essv5890823, essv5592861, essv6469261, essv6223982
SamplesHG00608, HG00702, HG00619, NA19084, NA19009, NA19072, HG00473, NA18622, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665445
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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