A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570704



Internal ID16011427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98648030..98650363hg38UCSC Ensembl
Innerchr15:99191259..99193592hg19UCSC Ensembl
Innerchr15:97008782..97011115hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382334
hg192334
hg182334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4766n54
Supporting Variantsnssv849607
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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