A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621529



Internal ID7008397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113090158..113120352hg38UCSC Ensembl
chr9:115852438..115882632hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3830195
hg1930195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606615, essv13606613, essv13606617, essv13606608, essv13606619, essv13606606, essv13606621, essv13606614, essv13606620, essv13606616, essv13606611, essv13606618, essv13606612, essv13606610, essv13606609, essv13606607, essv13606605
SamplesHG03096, NA19399, HG03115, NA19377, NA19038, HG03696, HG04047, HG03644, NA20126, NA18871, HG02666, NA19625, NA19380, HG02941, NA20807, NA18876, HG03072
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621529
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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