A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041671



Internal ID19130890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20534503..20559453hg38UCSC Ensembl
Innerchr16:20545825..20570775hg19UCSC Ensembl
Innerchr16:20453326..20478276hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3824951
hg1924951
hg1824951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3548039
Samples
Known GenesACSM2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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