A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551564



Internal ID16338973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78645142..78693691hg38UCSC Ensembl
Innerchr10:80404899..80453448hg19UCSC Ensembl
Innerchr10:80074905..80123454hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3848550
hg1948550
hg1848550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751744
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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