A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12460037



Internal ID2461853
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609913
Supporting Variants
SamplesHG03539
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12460037
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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