A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608101



Internal ID6995031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11911845..11916315hg38UCSC Ensembl
Innerchr6:11911861..11916300hg38UCSC Ensembl
Outerchr6:11911830..11916331hg38UCSC Ensembl
chr6:11912078..11916548hg19UCSC Ensembl
Innerchr6:11912094..11916533hg19UCSC Ensembl
Outerchr6:11912063..11916564hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg384471
hg194471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12189422
SamplesHG03781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608101
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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