A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061743



Internal ID19150962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33970586hg38UCSC Ensembl
Innerchr16:32280344..33773053hg19UCSC Ensembl
Innerchr16:32187845..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381701564
hg191492710
hg181492710
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3716347, nssv3550577, nssv3550578, nssv3550582, nssv3550576, nssv3550579, nssv3550580, nssv3550581, nssv3716346, nssv3550583
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)nsv1061743
Frequency
Sample Size11257
Observed Gain8
Observed Loss2
Observed Complex0
Frequencyn/a


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