A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064237



Internal ID18806768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21660605..22736323hg38UCSC Ensembl
Innerchr17:21564388..22235650hg19UCSC Ensembl
Innerchr17:21504981..22159777hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381075719
hg19671263
hg18654797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3128n100
Supporting Variantsnssv3561001
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064237
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