A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038800



Internal ID18781331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..171058hg38UCSC Ensembl
Innerchr16:60765..221057hg19UCSC Ensembl
Innerchr16:765..161057hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38160294
hg19160293
hg18160293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2690n100
Supporting Variantsnssv3556936
Samples
Known GenesDDX11L10, HBM, HBZ, 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)nsv1038800
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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