A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5869611



Internal ID9727963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96270221..96271564hg38UCSC Ensembl
Outerchr15:96270184..96271614hg38UCSC Ensembl
Innerchr15:96813450..96814793hg19UCSC Ensembl
Outerchr15:96813413..96814843hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381431
hg191431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668718
Supporting Variants
SamplesNA19651
Known GenesNR2F2-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5869611
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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