A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621818



Internal ID7008684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128799513..128813298hg38UCSC Ensembl
Innerchr9:128800013..128812798hg38UCSC Ensembl
Outerchr9:128798513..128814298hg38UCSC Ensembl
chr9:131561792..131575577hg19UCSC Ensembl
Innerchr9:131562292..131575077hg19UCSC Ensembl
Outerchr9:131560792..131576577hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813786
hg1913786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13625039
SamplesHG00632
Known GenesTBC1D13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621818
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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