A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571777



Internal ID16359186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28605736..28609990hg38UCSC Ensembl
Innerchr16:28617057..28621311hg19UCSC Ensembl
Innerchr16:28524558..28528812hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384255
hg194255
hg184255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv855421
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571777
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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