A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621401



Internal ID7008270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107652019..107666996hg38UCSC Ensembl
Innerchr9:107652519..107666496hg38UCSC Ensembl
Outerchr9:107651019..107667996hg38UCSC Ensembl
chr9:110414300..110429277hg19UCSC Ensembl
Innerchr9:110414800..110428777hg19UCSC Ensembl
Outerchr9:110413300..110430277hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3814978
hg1914978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13594411
SamplesHG02799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621401
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