A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621521



Internal ID6661700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112772842..112844016hg38UCSC Ensembl
chr9:115535122..115606296hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3871175
hg1971175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606325, essv13606318, essv13606321, essv13606316, essv13606320, essv13606319, essv13606322, essv13606323, essv13606326, essv13606317, essv13606314, essv13606324, essv13606315
SamplesNA19204, HG02337, HG03297, HG02541, HG03189, NA19209, NA18867, HG03169, NA19210, NA19391, HG01882, NA20126, NA18865
Known GenesSNX30
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621521
Frequency
Sample Size2504
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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