A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557299



Internal ID18508894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46161856..46596297hg38UCSC Ensembl
Innerchr17:44239222..44673663hg19UCSC Ensembl
Innerchr17:41594999..42028979hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38434442
hg19434442
hg18433981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066879
Supporting Variants
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, LRRC37A2, NSF, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557299
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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