A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059135



Internal ID19148354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84937418..84954615hg38UCSC Ensembl
Innerchr16:84971024..84988221hg19UCSC Ensembl
Innerchr16:83528525..83545722hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3817198
hg1917198
hg1817198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559963
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059135
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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