A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057713



Internal ID19146932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86729817..86762713hg38UCSC Ensembl
Innerchr16:86763423..86796319hg19UCSC Ensembl
Innerchr16:85320924..85353820hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3832897
hg1932897
hg1832897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3061n100
Supporting Variantsnssv3559978
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057713
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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