A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752186



Internal ID16046142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84654916..84724136hg38UCSC Ensembl
Innerchr10:86414672..86483892hg19UCSC Ensembl
Innerchr10:86404652..86473872hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3869221
hg1969221
hg1869221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551756
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)nssv752186
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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