A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621919



Internal ID6662095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132713668..132865324hg38UCSC Ensembl
Innerchr9:132713818..132865174hg38UCSC Ensembl
Outerchr9:132713518..132865474hg38UCSC Ensembl
chr9:135589055..135740711hg19UCSC Ensembl
Innerchr9:135589205..135740561hg19UCSC Ensembl
Outerchr9:135588905..135740861hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38151657
hg19151657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1513e214
Supporting Variantsessv13635933, essv13635934
SamplesHG01602, HG00131
Known GenesAK8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621919
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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