A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551810



Internal ID16339219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942633..86944294hg38UCSC Ensembl
Innerchr10:88702390..88704051hg19UCSC Ensembl
Innerchr10:88692370..88694031hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381662
hg191662
hg181662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752258
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551810
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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