A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551776



Internal ID16339185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86366236..86367529hg38UCSC Ensembl
Innerchr10:88125993..88127286hg19UCSC Ensembl
Innerchr10:88115973..88117266hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381294
hg191294
hg181294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1318n54
Supporting Variantsnssv752216, nssv752217
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551776
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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