A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063441



Internal ID18805972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88767066..88861882hg38UCSC Ensembl
Innerchr16:88833474..88928290hg19UCSC Ensembl
Innerchr16:87360975..87455791hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3894817
hg1994817
hg1894817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559999
Samples
Known GenesAPRT, CDT1, GALNS, PIEZO1, TRAPPC2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063441
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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