A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615209



Internal ID16402618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113090435..113104996hg38UCSC Ensembl
Innerchr9:115852715..115867276hg19UCSC Ensembl
Innerchr9:114892536..114907097hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3814562
hg1914562
hg1814562
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176137, nssv1141250, nssv1176128, nssv1141251, nssv1176136, nssv1176131, nssv1176132, nssv1141253, nssv1176129, nssv1141254, nssv1176133, nssv1141252, nssv1176135, nssv1176134, nssv1176130
SamplesHGDP00454, HGDP00918, HGDP00057, HGDP00216, HGDP00681, HGDP00160, HGDP00920, HGDP00906, HGDP01094, HGDP00931
Known GenesFAM225B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615209
Frequency
Sample Size17421
Observed Gain1
Observed Loss14
Observed Complex0
Frequencyn/a


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