A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11682148



Internal ID1683964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166083165..166083765hg38UCSC Ensembl
Innerchr4:166083165..166083765hg38UCSC Ensembl
Outerchr4:166083165..166083765hg38UCSC Ensembl
chr4:167004317..167004917hg19UCSC Ensembl
Innerchr4:167004317..167004917hg19UCSC Ensembl
Outerchr4:167004317..167004917hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603031
Supporting Variants
SamplesNA18634
Known GenesTLL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11682148
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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