A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565695



Internal ID7037077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:156356664..156367081hg38UCSC Ensembl
Outerchr2:157213176..157223593hg19UCSC Ensembl
Outerchr2:156921422..156931839hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3810418
hg1910418
hg1810418
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995163
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565695
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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