A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176492



Internal ID15507098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125641230..125704242hg38UCSC Ensembl
Innerchr9:128403509..128466521hg19UCSC Ensembl
Innerchr9:127443330..127506342hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3863013
hg1963013
hg1863013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615293
Supporting Variants
Samples1780854441_A
Known GenesMAPKAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176492
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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