A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893021



Internal ID18837155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46489976..46704811hg38UCSC Ensembl
Outerchr17:46474739..46704811hg38UCSC Ensembl
Innerchr17:44567342..44782177hg19UCSC Ensembl
Outerchr17:44552105..44782177hg19UCSC Ensembl
Innerchr17:41922658..42137359hg18UCSC Ensembl
Outerchr17:41907421..42137359hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38230073
hg19230073
hg18229939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788584, essv25792255, essv25792634, essv25790604, essv25791671, essv25789810, essv25789656, essv25790146, essv25788582, essv25788918, essv25791320
Samples
Known GenesARL17A, ARL17B, LRRC37A2, NSF, NSFP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893021
Frequency
Sample Size3017
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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