A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7761017



Internal ID12704202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71223769..71223770hg38UCSC Ensembl
Innerchr10:71223729..71223810hg38UCSC Ensembl
Outerchr10:71223728..71223811hg38UCSC Ensembl
chr10:72983526..72983527hg19UCSC Ensembl
Innerchr10:72983486..72983567hg19UCSC Ensembl
Outerchr10:72983485..72983568hg19UCSC Ensembl
chr10:72653532..72653533hg18UCSC Ensembl
Innerchr10:72653573..72653492hg18UCSC Ensembl
Outerchr10:72653491..72653574hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38142
hg19142
hg18142
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305960
Supporting Variants
SamplesNA07346
Known GenesUNC5B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7761017
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