A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055410



Internal ID19144629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62628255..62687066hg38UCSC Ensembl
Innerchr16:62662159..62720970hg19UCSC Ensembl
Innerchr16:61219660..61278471hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3858812
hg1958812
hg1858812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722721
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)nsv1055410
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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