A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12264110



Internal ID2884707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32058410..32059406hg38UCSC Ensembl
Innerchr6:32058560..32059256hg38UCSC Ensembl
Outerchr6:32058260..32059556hg38UCSC Ensembl
chr6:32026187..32027183hg19UCSC Ensembl
Innerchr6:32026337..32027033hg19UCSC Ensembl
Outerchr6:32026037..32027333hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608576
Supporting Variants
SamplesHG02558
Known GenesTNXB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12264110
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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