A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620975



Internal ID7007845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87060408..87068096hg38UCSC Ensembl
Innerchr9:87060408..87068096hg38UCSC Ensembl
Outerchr9:87060142..87068367hg38UCSC Ensembl
chr9:89675323..89683011hg19UCSC Ensembl
Innerchr9:89675323..89683011hg19UCSC Ensembl
Outerchr9:89675057..89683282hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387689
hg197689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13546988, essv13546989, essv13546993, essv13546996, essv13546998, essv13546991, essv13546995, essv13546994, essv13546990, essv13546997, essv13546992
SamplesHG03378, HG01462, HG03175, HG02870, NA18870, NA19247, HG02568, HG01915, HG02837, NA19713, HG02284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620975
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer