A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621518



Internal ID6661697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112634869..112691421hg38UCSC Ensembl
chr9:115397149..115453701hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3856553
hg1956553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606242, essv13606243, essv13606251, essv13606241, essv13606244, essv13606252, essv13606240, essv13606249, essv13606250, essv13606245, essv13606248, essv13606247, essv13606246
SamplesHG01882, NA19209, HG03189, NA18865, NA19210, HG03169, NA20126, HG02541, HG02337, HG03297, NA19391, NA18867, NA19204
Known GenesINIP, KIAA1958
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621518
Frequency
Sample Size2504
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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