A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041006



Internal ID18783537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..64016hg38UCSC Ensembl
Innerchr16:60765..114014hg19UCSC Ensembl
Innerchr16:765..54014hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3853252
hg1953250
hg1853250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2688n100
Supporting Variantsnssv3556927
Samples
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2, 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)nsv1041006
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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