A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062900



Internal ID18805431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70219926hg38UCSC Ensembl
Innerchr16:70049784..70253829hg19UCSC Ensembl
Innerchr16:68607285..68811330hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38204046
hg19204046
hg18204046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3006n100
Supporting Variantsnssv3559512
Samples
Known GenesCLEC18C, LOC100506060, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062900
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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