A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752689



Internal ID16046645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87516217..87516650hg38UCSC Ensembl
Innerchr10:89275974..89276407hg19UCSC Ensembl
Innerchr10:89265954..89266387hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38434
hg19434
hg18434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551829
Supporting Variants
Samples
Known GenesMINPP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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