A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551885



Internal ID16339294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90698132..90705170hg38UCSC Ensembl
Innerchr10:92457889..92464927hg19UCSC Ensembl
Innerchr10:92447869..92454907hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1339n54
Supporting Variantsnssv753335
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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