A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695163



Internal ID18993444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115693548..115836092hg38UCSC Ensembl
Innerchr9:118455827..118598371hg19UCSC Ensembl
Innerchr9:117495648..117638192hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38142545
hg19142545
hg18142545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047761
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)nssv3695163
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