A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048856



Internal ID19138075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126213032..126225619hg38UCSC Ensembl
Innerchr9:128975311..128987898hg19UCSC Ensembl
Innerchr9:128015132..128027719hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3812588
hg1912588
hg1812588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695246
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)nsv1048856
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