A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12567985



Internal ID3155064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140069691..140277411hg38UCSC Ensembl
chr6:140390828..140598548hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38207721
hg19207721
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610988
Supporting Variants
SamplesHG02778
Known GenesMIR3668
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12567985
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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