A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718829



Internal ID18670424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1505070..1866102hg38UCSC Ensembl
Innerchr16:1555071..1916103hg19UCSC Ensembl
Innerchr16:1495072..1856104hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38361033
hg19361033
hg18361033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051692
Supporting Variants
Samples
Known GenesCRAMP1L, EME2, FAHD1, HAGH, HN1L, IFT140, IGFALS, MAPK8IP3, MEIOB, MIR3177, MRPS34, NME3, NUBP2, SPSB3, TELO2, TMEM204
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718829
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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