A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752184



Internal ID16046140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84371303..84502050hg38UCSC Ensembl
Innerchr10:86131059..86261806hg19UCSC Ensembl
Innerchr10:86121039..86251786hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38130748
hg19130748
hg18130748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551754
Supporting Variants
Samples
Known GenesCCSER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752184
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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