A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659192



Internal ID9925297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27629801..27635140hg38UCSC Ensembl
Outerchr9:27629767..27635175hg38UCSC Ensembl
Innerchr9:27629799..27635138hg19UCSC Ensembl
Outerchr9:27629765..27635173hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385409
hg195409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1332e199
Supporting Variantsessv5577120
SamplesHG00120
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659192
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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