A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035156



Internal ID18777687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5091032..5996934hg38UCSC Ensembl
Innerchr16:5141033..6046935hg19UCSC Ensembl
Innerchr16:5081034..5986936hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38905903
hg19905903
hg18905903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556979
Samples
Known GenesFAM86A, MIR8065
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035156
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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