A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621864



Internal ID7008730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130639934..130655579hg38UCSC Ensembl
Innerchr9:130639956..130655558hg38UCSC Ensembl
Outerchr9:130639913..130655601hg38UCSC Ensembl
chr9:133515321..133530966hg19UCSC Ensembl
Innerchr9:133515343..133530945hg19UCSC Ensembl
Outerchr9:133515300..133530988hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3815646
hg1915646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13630357
SamplesHG04006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621864
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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