A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29985



Internal ID12608179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38228794..38319127hg38UCSC Ensembl
Innerchr7:38268395..38358728hg19UCSC Ensembl
Innerchr7:38234920..38325253hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3890334
hg1990334
hg1890334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84224
SamplesHuRef
Known GenesSTARD3NL, TARP
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29985
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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