A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064291



Internal ID19153510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13275120..13330887hg38UCSC Ensembl
Innerchr17:13178437..13234204hg19UCSC Ensembl
Innerchr17:13119162..13174929hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3855768
hg1955768
hg1855768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3100n100
Supporting Variantsnssv3560356, nssv3719171, nssv3719170, nssv3560357, nssv3560355
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)nsv1064291
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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