A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061610



Internal ID19150829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32369618..33800658hg38UCSC Ensembl
Innerchr16:32380939..33603125hg19UCSC Ensembl
Innerchr16:32288440..33510626hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381431041
hg191222187
hg181222187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n100
Supporting Variantsnssv3716373, nssv3551089, nssv3716374
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)nsv1061610
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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