A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622041



Internal ID6662211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137686055..137702179hg38UCSC Ensembl
Innerchr9:137686555..137701679hg38UCSC Ensembl
Outerchr9:137685055..137703179hg38UCSC Ensembl
chr9:140580507..140596631hg19UCSC Ensembl
Innerchr9:140581007..140596131hg19UCSC Ensembl
Outerchr9:140579507..140597631hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3816125
hg1916125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13660500, essv13660499, essv13660501
SamplesHG01342, NA19917, HG02819
Known GenesEHMT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622041
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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