A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11681036



Internal ID1682852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165996732..166000406hg38UCSC Ensembl
Innerchr4:165996752..166000387hg38UCSC Ensembl
Outerchr4:165996713..166000426hg38UCSC Ensembl
chr4:166917884..166921558hg19UCSC Ensembl
Innerchr4:166917904..166921539hg19UCSC Ensembl
Outerchr4:166917865..166921578hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg383675
hg193675
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603030
Supporting Variants
SamplesHG02734
Known GenesTLL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11681036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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