A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060504



Internal ID19149723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35334296..35418187hg38UCSC Ensembl
Innerchr16:34568667..34652558hg19UCSC Ensembl
Innerchr16:34426168..34510059hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3883892
hg1983892
hg1883892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2969n100
Supporting Variantsnssv3559148
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)nsv1060504
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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