A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621531



Internal ID6661709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113092119..113112981hg38UCSC Ensembl
Innerchr9:113092119..113112981hg38UCSC Ensembl
Outerchr9:113092016..113113112hg38UCSC Ensembl
chr9:115854399..115875261hg19UCSC Ensembl
Innerchr9:115854399..115875261hg19UCSC Ensembl
Outerchr9:115854296..115875392hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3820863
hg1920863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606649, essv13606659, essv13606645, essv13606650, essv13606643, essv13606657, essv13606658, essv13606646, essv13606656, essv13606652, essv13606648, essv13606655, essv13606662, essv13606653, essv13606647, essv13606651, essv13606660, essv13606661, essv13606644, essv13606654
SamplesHG02666, NA19625, NA18871, HG03696, NA19467, NA19443, NA20807, NA18876, HG02941, NA19377, NA19380, NA20126, HG03096, HG03072, HG03115, NA19038, HG04047, HG03644, HG01593, NA19399
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621531
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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