A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050826



Internal ID19140045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137325391..137378611hg38UCSC Ensembl
Innerchr9:140219843..140273063hg19UCSC Ensembl
Innerchr9:139339664..139392884hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3853221
hg1953221
hg1853221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696513
Samples
Known GenesEXD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050826
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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