A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021668



Internal ID19110886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28587996..28765785hg38UCSC Ensembl
Innerchr9:28587994..28765783hg19UCSC Ensembl
Innerchr9:28577994..28755783hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38177790
hg19177790
hg18177790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7491n100
Supporting Variantsnssv3692046, nssv3692045
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021668
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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