A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550853



Internal ID15991576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46001360..46085061hg38UCSC Ensembl
Innerchr10:51510761..51594462hg19UCSC Ensembl
Innerchr10:51180767..51264468hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3883702
hg1983702
hg1883702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174542
SamplesHGDP00986
Known GenesMSMB, NCOA4, TIMM23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550853
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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