A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571406



Internal ID16012129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8596737..8690609hg38UCSC Ensembl
Innerchr16:8690594..8784466hg19UCSC Ensembl
Innerchr16:8598095..8691967hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3893873
hg1993873
hg1893873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852424
Samples
Known GenesABAT, METTL22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571406
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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