A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621088



Internal ID7007958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92777849..92801795hg38UCSC Ensembl
Innerchr9:92777849..92801795hg38UCSC Ensembl
Outerchr9:92777349..92802295hg38UCSC Ensembl
chr9:95540131..95564077hg19UCSC Ensembl
Innerchr9:95540131..95564077hg19UCSC Ensembl
Outerchr9:95539631..95564577hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3823947
hg1923947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559477
SamplesHG02820
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621088
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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