A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620544



Internal ID6660726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68432383..68585491hg38UCSC Ensembl
chr9:71047299..71200407hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38153109
hg19153109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13504905, essv13504904
SamplesHG03729, HG03788
Known GenesLOC101927015, PGM5, TMEM252
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620544
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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