A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574956



Internal ID16015679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37779417..37852040hg38UCSC Ensembl
Innerchr17:36139387..36211659hg19UCSC Ensembl
Innerchr17:33213500..33285772hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3872624
hg1972273
hg1872273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870489
Samples
Known GenesYWHAEP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574956
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