A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551477



Internal ID16338886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69751325..69773286hg38UCSC Ensembl
Innerchr10:71511081..71533042hg19UCSC Ensembl
Innerchr10:71181087..71203048hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3821962
hg1921962
hg1821962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750120
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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