A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674813



Internal ID9940918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28174241..28679242hg38UCSC Ensembl
Outerchr15:28174207..28679277hg38UCSC Ensembl
Innerchr15:28419387..28924388hg19UCSC Ensembl
Outerchr15:28419353..28924423hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38505071
hg19505071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6229315
SamplesHG00437
Known GenesGOLGA8F, GOLGA8G, HERC2, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674813
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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