A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056958



Internal ID18799489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70015881..70153279hg38UCSC Ensembl
Innerchr16:70049784..70187182hg19UCSC Ensembl
Innerchr16:68607285..68744683hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38137399
hg19137399
hg18137399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3004n100
Supporting Variantsnssv3559502
Samples
Known GenesMIR1972-1, 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)nsv1056958
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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