A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551061



Internal ID16338470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56415869..56580431hg38UCSC Ensembl
Innerchr10:58175630..58340191hg19UCSC Ensembl
Innerchr10:57845636..58010197hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38164563
hg19164562
hg18164562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748559
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551061
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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