A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6174982



Internal ID9815940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130547423..130550406hg38UCSC Ensembl
Outerchr9:130547266..130550559hg38UCSC Ensembl
Innerchr9:133422810..133425793hg19UCSC Ensembl
Outerchr9:133422653..133425946hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383294
hg193294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657887
Supporting Variants
SamplesNA19982
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6174982
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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