A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046002



Internal ID19135221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12388146..12416786hg38UCSC Ensembl
Innerchr16:12482003..12510643hg19UCSC Ensembl
Innerchr16:12389504..12418144hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3828641
hg1928641
hg1828641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557147
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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