A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570698



Internal ID16358107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647653..98650539hg38UCSC Ensembl
Innerchr15:99190882..99193768hg19UCSC Ensembl
Innerchr15:97008405..97011291hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382887
hg192887
hg182887
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4764n54
Supporting Variantsnssv849601, nssv849600
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570698
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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