A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673315



Internal ID9939420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35179956..35187854hg38UCSC Ensembl
Outerchr18:35179919..35187904hg38UCSC Ensembl
Innerchr18:32759920..32767818hg19UCSC Ensembl
Outerchr18:32759883..32767868hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg387986
hg197986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6127368
SamplesNA19138
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673315
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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