A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057411



Internal ID19146630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35305358..35383152hg38UCSC Ensembl
Innerchr16:34539729..34617523hg19UCSC Ensembl
Innerchr16:34397230..34475024hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3877795
hg1977795
hg1877795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2967n100
Supporting Variantsnssv3559070
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057411
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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