A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059278



Internal ID18801809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21623779..22736323hg38UCSC Ensembl
Innerchr17:21527046..22235650hg19UCSC Ensembl
Innerchr17:21467639..22159777hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381112545
hg19708605
hg18692139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3128n100
Supporting Variantsnssv3720036, nssv3560997, nssv3560996
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)nsv1059278
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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