A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891724



Internal ID19186120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118932967..118979938hg38UCSC Ensembl
Outerchr9:118932967..118979938hg38UCSC Ensembl
Innerchr9:121695245..121742216hg19UCSC Ensembl
Outerchr9:121695245..121742216hg19UCSC Ensembl
Innerchr9:120735066..120782037hg18UCSC Ensembl
Outerchr9:120735066..120782037hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3846972
hg1946972
hg1846972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798338
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891724
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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