A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620685



Internal ID7007555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73939094..74014405hg38UCSC Ensembl
chr9:76554010..76629321hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3875312
hg1975312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13520049
SamplesHG01865
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620685
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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