A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574142



Internal ID16361551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:958293..1008054hg38UCSC Ensembl
Innerchr17:861533..911294hg19UCSC Ensembl
Innerchr17:808283..858044hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3849762
hg1949762
hg1849762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866247
Samples
Known GenesABR, NXN, TIMM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574142
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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