A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559999



Internal ID18511594
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 StatusS
Merged Variantsnsv1063441
Supporting Variants
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)nssv3559999
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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