A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608390



Internal ID6995320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25703661..25707545hg38UCSC Ensembl
Innerchr6:25703661..25707545hg38UCSC Ensembl
Outerchr6:25703488..25707726hg38UCSC Ensembl
chr6:25703889..25707773hg19UCSC Ensembl
Innerchr6:25703889..25707773hg19UCSC Ensembl
Outerchr6:25703716..25707954hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg383885
hg193885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12232479
SamplesNA19712
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608390
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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