A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564676



Internal ID7035776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35620317..35625382hg38UCSC Ensembl
Outerchr10:35909245..35914310hg19UCSC Ensembl
Outerchr10:35949251..35954316hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385066
hg195066
hg185066
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010054
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564676
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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