A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615417



Internal ID16402826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129142057..129198591hg38UCSC Ensembl
Innerchr9:131904336..131960870hg19UCSC Ensembl
Innerchr9:130944157..131000691hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3856535
hg1956535
hg1856535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1143574
Samples
Known GenesIER5L, PPP2R4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615417
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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