A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565765



Internal ID7037147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:86985681..86986771hg38UCSC Ensembl
Outerchr7:86614997..86616087hg19UCSC Ensembl
Outerchr7:86452933..86454023hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998639
Supporting Variants
SamplesHuRef
Known GenesKIAA1324L
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565765
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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