A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610615



Internal ID6997532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122639341..122665870hg38UCSC Ensembl
Innerchr6:122639344..122665867hg38UCSC Ensembl
Outerchr6:122639338..122665873hg38UCSC Ensembl
chr6:122960486..122987015hg19UCSC Ensembl
Innerchr6:122960489..122987012hg19UCSC Ensembl
Outerchr6:122960483..122987018hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3826530
hg1926530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12527186, essv12527187, essv12527185
SamplesHG03914, HG03809, HG03692
Known GenesPKIB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610615
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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