A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587156



Internal ID7058538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73417138..73418308hg38UCSC Ensembl
Innerchr7:72831468..72832638hg19UCSC Ensembl
Innerchr7:72469404..72470574hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381171
hg191171
hg181171
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998241
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587156
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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