A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725548



Internal ID18677143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46270361..46707300hg38UCSC Ensembl
Innerchr17:44347727..44784666hg19UCSC Ensembl
Innerchr17:41703504..42139849hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38436940
hg19436940
hg18436346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060420
Supporting Variants
Samples
Known GenesARL17A, ARL17B, 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)nssv3725548
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