A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551057



Internal ID16338466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56161402..56303585hg38UCSC Ensembl
Innerchr10:57921163..58063346hg19UCSC Ensembl
Innerchr10:57591169..57733352hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38142184
hg19142184
hg18142184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1180n54
Supporting Variantsnssv748555
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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