A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552054



Internal ID16339463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101277891..101326146hg38UCSC Ensembl
Innerchr10:103037648..103085903hg19UCSC Ensembl
Innerchr10:103027638..103075893hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3848256
hg1948256
hg1848256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv756074
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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