A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673169



Internal ID9939274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125163572..125168861hg38UCSC Ensembl
Outerchr9:125163535..125168911hg38UCSC Ensembl
Innerchr9:127925851..127931140hg19UCSC Ensembl
Outerchr9:127925814..127931190hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385377
hg195377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6318698
SamplesHG00476
Known GenesPPP6C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673169
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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