A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044146



Internal ID19133365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108304789..108390861hg38UCSC Ensembl
Innerchr9:111067069..111153141hg19UCSC Ensembl
Innerchr9:110106890..110192962hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3886073
hg1986073
hg1886073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697649
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044146
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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