A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044983



Internal ID19134202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20534503..20568633hg38UCSC Ensembl
Innerchr16:20545825..20579955hg19UCSC Ensembl
Innerchr16:20453326..20487456hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3834131
hg1934131
hg1834131
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3548042, nssv3548044, nssv3548045, nssv3548040, nssv3548043, nssv3548041
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)nsv1044983
Frequency
Sample Size11257
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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