A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575587



Internal ID16362996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53624699..53676156hg38UCSC Ensembl
Innerchr17:51702060..51753517hg19UCSC Ensembl
Innerchr17:49057059..49108516hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3851458
hg1951458
hg1851458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873570
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575587
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