A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559996



Internal ID18511591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88711587..88907529hg38UCSC Ensembl
Innerchr16:88777995..88973937hg19UCSC Ensembl
Innerchr16:87305496..87501438hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38195943
hg19195943
hg18195943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055581
Supporting Variants
Samples
Known GenesAPRT, CBFA2T3, CDT1, CTU2, GALNS, LOC100289580, MIR4722, PABPN1L, 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)nssv3559996
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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