A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060794



Internal ID19150013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35294244..35376417hg38UCSC Ensembl
Innerchr16:34528615..34610788hg19UCSC Ensembl
Innerchr16:34386116..34468289hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3882174
hg1982174
hg1882174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2967n100
Supporting Variantsnssv3559038
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)nsv1060794
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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