A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550222



Internal ID16337631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24234860..24257812hg38UCSC Ensembl
Innerchr10:24523789..24546741hg19UCSC Ensembl
Innerchr10:24563795..24586747hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3822953
hg1922953
hg1822953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744734
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550222
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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