A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621530



Internal ID6661708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113090158..113120352hg38UCSC Ensembl
chr9:115852438..115882632hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3830195
hg1930195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606639, essv13606624, essv13606622, essv13606635, essv13606638, essv13606626, essv13606640, essv13606642, essv13606627, essv13606631, essv13606633, essv13606625, essv13606629, essv13606623, essv13606641, essv13606636, essv13606630, essv13606637, essv13606628, essv13606632, essv13606634
SamplesHG02793, HG01873, HG03703, HG04229, HG02156, HG00592, HG04238, HG04210, NA18624, HG03021, NA18635, HG01795, HG01867, HG02073, HG04134, HG01632, NA18565, HG04018, HG00476, HG02774, HG02179
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621530
Frequency
Sample Size2504
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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