A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609913



Internal ID6650141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90035116..90104866hg38UCSC Ensembl
Innerchr6:90035116..90104866hg38UCSC Ensembl
Outerchr6:90034616..90105366hg38UCSC Ensembl
chr6:90744835..90814585hg19UCSC Ensembl
Innerchr6:90744835..90814585hg19UCSC Ensembl
Outerchr6:90744335..90815085hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3869751
hg1969751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12460037
SamplesHG03539
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609913
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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