A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050325



Internal ID18792856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954899..15166867hg38UCSC Ensembl
Innerchr16:15048756..15260724hg19UCSC Ensembl
Innerchr16:14956257..15168225hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38211969
hg19211969
hg18211969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557796
Samples
Known GenesMIR1972-1, MIR1972-2, MIR3180-4, MIR6511B-1, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050325
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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