A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571238



Internal ID16358647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2648856..2663274hg38UCSC Ensembl
Innerchr16:2698857..2713275hg19UCSC Ensembl
Innerchr16:2638858..2653276hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814419
hg1914419
hg1814419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4870n54
Supporting Variantsnssv852248
Samples
Known GenesERVK13-1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571238
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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