A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060540



Internal ID18803071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34208804..36048843hg38UCSC Ensembl
Innerchr16:34011271..35283214hg19UCSC Ensembl
Innerchr16:33918772..35140715hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg381840040
hg191271944
hg181221944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2960n100
Supporting Variantsnssv3556008
Samples
Known GenesFLJ26245, LOC100130700, LOC146481, LOC283914, UBE2MP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060540
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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