A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058226



Internal ID19147445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:51725226..51745916hg38UCSC Ensembl
Innerchr16:51759137..51779827hg19UCSC Ensembl
Innerchr16:50316638..50337328hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3820691
hg1920691
hg1820691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2978n100
Supporting Variantsnssv3559259
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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