A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575175



Internal ID16015898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46143895..46437877hg38UCSC Ensembl
Innerchr17:44221261..44515243hg19UCSC Ensembl
Innerchr17:41577038..41870683hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38293983
hg19293983
hg18293646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5623n54
Supporting Variantsnssv872412
Samples
Known GenesARL17A, ARL17B, KANSL1, KANSL1-AS1, LOC644172, LRRC37A, NSFP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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