A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752233



Internal ID15699503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86656141..86657967hg38UCSC Ensembl
Innerchr10:88415898..88417724hg19UCSC Ensembl
Innerchr10:88405878..88407704hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381827
hg191827
hg181827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551792
Supporting Variants
Samples
Known GenesOPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752233
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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