A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837024



Internal ID15038268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36670765..36670766hg38UCSC Ensembl
Innerchr9:36670737..36670794hg38UCSC Ensembl
Outerchr9:36670736..36670795hg38UCSC Ensembl
chr9:36670762..36670763hg19UCSC Ensembl
Innerchr9:36670734..36670791hg19UCSC Ensembl
Outerchr9:36670733..36670792hg19UCSC Ensembl
chr9:36660762..36660763hg18UCSC Ensembl
Innerchr9:36660791..36660734hg18UCSC Ensembl
Outerchr9:36660733..36660792hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38205
hg19205
hg18205
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308549
Supporting Variants
SamplesNA19239
Known GenesMELK
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837024
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