A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564971



Internal ID7036071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:47663540..47664377hg38UCSC Ensembl
Outerchr7:47703138..47703975hg19UCSC Ensembl
Outerchr7:47669663..47670500hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38838
hg19838
hg18838
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009681
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564971
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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