A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7801624



Internal ID13077724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87276755..87276756hg38UCSC Ensembl
Innerchr9:87276734..87276777hg38UCSC Ensembl
Outerchr9:87276733..87276778hg38UCSC Ensembl
chr9:89891670..89891671hg19UCSC Ensembl
Innerchr9:89891649..89891692hg19UCSC Ensembl
Outerchr9:89891648..89891693hg19UCSC Ensembl
chr9:89081490..89081491hg18UCSC Ensembl
Innerchr9:89081512..89081469hg18UCSC Ensembl
Outerchr9:89081468..89081513hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386040
hg196040
hg186040
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303982
Supporting Variants
SamplesNA07347
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7801624
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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