A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620662



Internal ID6660843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73155774..73254536hg38UCSC Ensembl
chr9:75770690..75869452hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3898763
hg1998763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13518584
SamplesHG00276
Known GenesANXA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620662
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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