A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574614



Internal ID16362023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22409941..22568765hg38UCSC Ensembl
Innerchr17:21909270..22068092hg19UCSC Ensembl
Innerchr17:21833397..21992219hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38158825
hg19158823
hg18158823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149352
SamplesHGDP01053
Known GenesFLJ36000, MTRNR2L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574614
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