A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657920



Internal ID9924025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32711099..32729723hg38UCSC Ensembl
Outerchr9:32711065..32729758hg38UCSC Ensembl
Innerchr9:32711097..32729721hg19UCSC Ensembl
Outerchr9:32711063..32729756hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3818694
hg1918694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1334e199
Supporting Variantsessv5545998
SamplesHG00265
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657920
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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