A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570696



Internal ID16358105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647653..98650200hg38UCSC Ensembl
Innerchr15:99190882..99193429hg19UCSC Ensembl
Innerchr15:97008405..97010952hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382548
hg192548
hg182548
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4764n54
Supporting Variantsnssv849594, nssv849597, nssv849595, nssv849593, nssv849596, nssv849592
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570696
Frequency
Sample Size17421
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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