A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000677



Internal ID7065807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:107184607..107195967hg38UCSC Ensembl
Outerchr6:107505811..107517171hg19UCSC Ensembl
Outerchr6:107612504..107623864hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811361
hg1911361
hg1811361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565822
SamplesHuRef
Known GenesPDSS2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000677
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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