A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672037



Internal ID9938142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26896112..26902793hg38UCSC Ensembl
Outerchr9:26896075..26902843hg38UCSC Ensembl
Innerchr9:26896110..26902791hg19UCSC Ensembl
Outerchr9:26896073..26902841hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg386769
hg196769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6544467
SamplesHG00338
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672037
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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