A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058908



Internal ID19148127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..33561486hg38UCSC Ensembl
Innerchr16:32080861..33363953hg19UCSC Ensembl
Innerchr16:31988362..33271454hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381491947
hg191283093
hg181283093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2842n100
Supporting Variantsnssv3549355
Samples
Known GenesHERC2P4, LOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058908
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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