A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563916



Internal ID7035016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:35136385..35137443hg38UCSC Ensembl
Outerchr6:35104162..35105220hg19UCSC Ensembl
Outerchr6:35212140..35213198hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381059
hg191059
hg181059
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001098
Supporting Variants
SamplesHuRef
Known GenesTCP11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563916
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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