A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551881



Internal ID15992604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90331028..90697976hg38UCSC Ensembl
Innerchr10:92090785..92457733hg19UCSC Ensembl
Innerchr10:92080765..92447713hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38366949
hg19366949
hg18366949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1338n54
Supporting Variantsnssv753331
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551881
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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