A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620597



Internal ID7007467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71134764..71183181hg38UCSC Ensembl
chr9:73749680..73798097hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3848418
hg1948418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13513349
SamplesNA19678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620597
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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