A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753224



Internal ID15700494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88999967..89015999hg38UCSC Ensembl
Innerchr10:90759724..90775756hg19UCSC Ensembl
Innerchr10:90749704..90765736hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3816033
hg1916033
hg1816033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551841
Supporting Variants
Samples
Known GenesFAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753224
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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