A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3248n100



Internal ID20154864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46267481..46596297hg38UCSC Ensembl
chr17:44344847..44673663hg19UCSC Ensembl
chr17:41700624..42028979hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38328817
hg19328817
hg18328356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065393, nsv1057064, nsv1056215, nsv1055434, nsv1057050, nsv1058499, nsv1062988, nsv1056925, nsv1064352, nsv1063729, nsv1066703, nsv1057394, nsv1058752
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)dgv3248n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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