A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv745548



Internal ID15692818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28052854..28111906hg38UCSC Ensembl
Innerchr10:28341783..28400835hg19UCSC Ensembl
Innerchr10:28381789..28440841hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3859053
hg1959053
hg1859053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550284
Supporting Variants
Samples
Known GenesMPP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv745548
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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