A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551454



Internal ID16338863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69495991..69531984hg38UCSC Ensembl
Innerchr10:71255747..71291740hg19UCSC Ensembl
Innerchr10:70925753..70961746hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3835994
hg1935994
hg1835994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174237
Samples1798860587_A
Known GenesTSPAN15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551454
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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