A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12232480



Internal ID5420684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25893685..25905376hg38UCSC Ensembl
Innerchr6:25893694..25905368hg38UCSC Ensembl
Outerchr6:25893677..25905385hg38UCSC Ensembl
chr6:25893913..25905604hg19UCSC Ensembl
Innerchr6:25893922..25905596hg19UCSC Ensembl
Outerchr6:25893905..25905613hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3811692
hg1911692
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608391
Supporting Variants
SamplesNA18951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12232480
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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