A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621663



Internal ID7008531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121461112..121468993hg38UCSC Ensembl
Innerchr9:121461162..121468943hg38UCSC Ensembl
Outerchr9:121461062..121469043hg38UCSC Ensembl
chr9:124223390..124231271hg19UCSC Ensembl
Innerchr9:124223440..124231221hg19UCSC Ensembl
Outerchr9:124223340..124231321hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg387882
hg197882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13615519
SamplesNA19138
Known GenesGGTA1P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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