A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615601



Internal ID16056324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133071778..133082065hg38UCSC Ensembl
Innerchr9:135947165..135957452hg19UCSC Ensembl
Innerchr9:134936986..134947273hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3810288
hg1910288
hg1810288
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145389, nssv1145388
Samples
Known GenesCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615601
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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