A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571527



Internal ID16012250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15031584..15074903hg38UCSC Ensembl
Innerchr16:15125441..15168760hg19UCSC Ensembl
Innerchr16:15032942..15076261hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3843320
hg1943320
hg1843320
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150544, nssv1150545, nssv1150543, nssv852803
Samples1780862015_A, 1782681079_A, HGDP00005
Known GenesNTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571527
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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