A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570699



Internal ID16011422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647822..98650200hg38UCSC Ensembl
Innerchr15:99191051..99193429hg19UCSC Ensembl
Innerchr15:97008574..97010952hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382379
hg192379
hg182379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4763n54
Supporting Variantsnssv849602
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570699
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