A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061064



Internal ID19150283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82131709..82180194hg38UCSC Ensembl
Innerchr16:82165314..82213799hg19UCSC Ensembl
Innerchr16:80722815..80771300hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3848486
hg1948486
hg1848486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3050n100
Supporting Variantsnssv3559843
Samples
Known GenesMPHOSPH6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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