A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753956



Internal ID15701226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92045217..92076212hg38UCSC Ensembl
Innerchr10:93804974..93835969hg19UCSC Ensembl
Innerchr10:93794954..93825949hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3830996
hg1930996
hg1830996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551923
Supporting Variants
Samples
Known GenesCPEB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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