A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061306



Internal ID19150525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55093104..55108806hg38UCSC Ensembl
Innerchr16:55127016..55142718hg19UCSC Ensembl
Innerchr16:53684517..53700219hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3815703
hg1915703
hg1815703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559274
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)nsv1061306
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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