A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039492



Internal ID19128711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12082660..12116845hg38UCSC Ensembl
Innerchr16:12176517..12210702hg19UCSC Ensembl
Innerchr16:12084018..12118203hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3834186
hg1934186
hg1834186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557143
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)nsv1039492
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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