A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675528



Internal ID9941633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88516047..88518652hg38UCSC Ensembl
Outerchr9:88515890..88518805hg38UCSC Ensembl
Innerchr9:91130962..91133567hg19UCSC Ensembl
Outerchr9:91130805..91133720hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382916
hg192916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1358e199
Supporting Variantsessv5757369, essv6308130
SamplesNA19678, HG00657
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675528
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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