A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550855



Internal ID15991578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50505505..50529904hg38UCSC Ensembl
Innerchr10:52265265..52289664hg19UCSC Ensembl
Innerchr10:51935271..51959670hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3824400
hg1924400
hg1824400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174543
SamplesHGDP00262
Known GenesSGMS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550855
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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