A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611217



Internal ID6998128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149932006..149949552hg38UCSC Ensembl
Innerchr6:149932006..149949552hg38UCSC Ensembl
Outerchr6:149931506..149950052hg38UCSC Ensembl
chr6:150253142..150270688hg19UCSC Ensembl
Innerchr6:150253142..150270688hg19UCSC Ensembl
Outerchr6:150252642..150271188hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3817547
hg1917547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12581128
SamplesNA20318
Known GenesULBP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611217
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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