A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570695



Internal ID16011418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647653..98650047hg38UCSC Ensembl
Innerchr15:99190882..99193276hg19UCSC Ensembl
Innerchr15:97008405..97010799hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382395
hg192395
hg182395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4763n54
Supporting Variantsnssv849591, nssv849590
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570695
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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