A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061329



Internal ID19150548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32553179..33908301hg38UCSC Ensembl
Innerchr16:32564500..33710768hg19UCSC Ensembl
Innerchr16:32472001..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381355123
hg191146269
hg181146269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2876n100
Supporting Variantsnssv3551901
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061329
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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