A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617169



Internal ID7004055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50352239..50373358hg38UCSC Ensembl
chr8:51264799..51285918hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3821120
hg1921120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1397e214
Supporting Variantsessv13197453
SamplesHG02756
Known GenesSNTG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617169
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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