A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3337917



Internal ID14838187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91296197..91296203hg38UCSC Ensembl
Innerchr9:91296189..91296209hg38UCSC Ensembl
Outerchr9:91296185..91296215hg38UCSC Ensembl
chr9:94058479..94058485hg19UCSC Ensembl
Innerchr9:94058471..94058491hg19UCSC Ensembl
Outerchr9:94058467..94058497hg19UCSC Ensembl
chr9:93098300..93098306hg18UCSC Ensembl
Innerchr9:93098312..93098292hg18UCSC Ensembl
Outerchr9:93098288..93098318hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8945501, essv8945484, essv8945493, essv8945491, essv8945483, essv8945485, essv8945473, essv8945495, essv8945497, essv8945474, essv8945472, essv8945498, essv8945499, essv8945480, essv8945496, essv8945479, essv8945482, essv8945502, essv8945471, essv8945488, essv8945477, essv8945489, essv8945476, essv8945478, essv8945486, essv8945487, essv8945490, essv8945494, essv8945500, essv8945475
SamplesNA18605, NA18951, NA18952, NA18526, NA18570, NA18948, NA18947, NA18573, NA18608, NA18965, NA11919, NA12763, NA18566, NA12155, NA18576, NA18960, NA18563, NA18592, NA18638, NA18959, NA18973, NA11995, NA18537, NA18558, NA18942, NA18940, NA18582, NA18552, NA18577, NA18532
Known GenesAUH
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3337917
Frequency
Sample Size185
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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