A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045829



Internal ID18788360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..95886hg38UCSC Ensembl
Innerchr16:60765..145884hg19UCSC Ensembl
Innerchr16:765..85884hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3885122
hg1985120
hg1885120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556933
Samples
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2, MPG, NPRL3, POLR3K, RHBDF1, SNRNP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045829
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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