A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1121105



Internal ID15974291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128751049..128761210hg38UCSC Ensembl
Innerchr8:129763295..129773456hg19UCSC Ensembl
Innerchr8:129832477..129842638hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3810162
hg1910162
hg1810162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612204
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1121105
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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