A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672659



Internal ID9938764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34726223..34835267hg38UCSC Ensembl
Outerchr9:34726189..34835302hg38UCSC Ensembl
Innerchr9:34726220..34835264hg19UCSC Ensembl
Outerchr9:34726186..34835299hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38109114
hg19109114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1337e199
Supporting Variantsessv6225589
SamplesNA19074
Known GenesFAM205A, FAM205B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672659
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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