A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611288



Internal ID6998197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152835140..152853205hg38UCSC Ensembl
Innerchr6:152835196..152853149hg38UCSC Ensembl
Outerchr6:152835084..152853261hg38UCSC Ensembl
chr6:153156275..153174340hg19UCSC Ensembl
Innerchr6:153156331..153174284hg19UCSC Ensembl
Outerchr6:153156219..153174396hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3818066
hg1918066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12586223
SamplesNA18573
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611288
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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