A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565567



Internal ID7036949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:92374497..92379567hg38UCSC Ensembl
Outerchr10:94134254..94139324hg19UCSC Ensembl
Outerchr10:94124234..94129304hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385071
hg195071
hg185071
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009764
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565567
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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