A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559995



Internal ID18511590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88711587..88886496hg38UCSC Ensembl
Innerchr16:88777995..88952904hg19UCSC Ensembl
Innerchr16:87305496..87480405hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38174910
hg19174910
hg18174910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059030
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)nssv3559995
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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