A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695239



Internal ID18993520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126000791..126072015hg38UCSC Ensembl
Innerchr9:128763070..128834294hg19UCSC Ensembl
Innerchr9:127802891..127874115hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3871225
hg1971225
hg1871225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046564
Supporting Variants
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)nssv3695239
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