A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997444



Internal ID7063783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:41411888..41423732hg38UCSC Ensembl
Outerchr6:41379626..41391470hg19UCSC Ensembl
Outerchr6:41487604..41499448hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3811845
hg1911845
hg1811845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565290
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997444
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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