A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607985



Internal ID6994916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5920128..5924106hg38UCSC Ensembl
Innerchr6:5920134..5924100hg38UCSC Ensembl
Outerchr6:5920122..5924112hg38UCSC Ensembl
chr6:5920361..5924339hg19UCSC Ensembl
Innerchr6:5920367..5924333hg19UCSC Ensembl
Outerchr6:5920355..5924345hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383979
hg193979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12180884, essv12180885, essv12180886, essv12180887
SamplesHG02250, HG02383, HG02155, HG02364
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607985
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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