A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585640



Internal ID347219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131167519..131168748hg38UCSC Ensembl
Outerchr9:131166881..131170147hg38UCSC Ensembl
Innerchr9:134042906..134044135hg19UCSC Ensembl
Outerchr9:134042268..134045534hg19UCSC Ensembl
Innerchr9:133032727..133033956hg18UCSC Ensembl
Outerchr9:133032089..133035355hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383267
hg193267
hg183267
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275417
Supporting Variants
Samples
Known GenesNUP214
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585640
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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