A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6037495



Internal ID9014898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141519577..141526850hg38UCSC Ensembl
Outerchr3:141519540..141526900hg38UCSC Ensembl
Innerchr3:141238419..141245692hg19UCSC Ensembl
Outerchr3:141238382..141245742hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg387361
hg197361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676781
Supporting Variants
SamplesHG00530
Known GenesRASA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6037495
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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