A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571576



Internal ID16012299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:17293303..17351178hg38UCSC Ensembl
Innerchr16:17387160..17445035hg19UCSC Ensembl
Innerchr16:17294661..17352536hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3857876
hg1957876
hg1857876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852866
Samples
Known GenesXYLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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