A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063685



Internal ID19152904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62094105..62188974hg38UCSC Ensembl
Innerchr16:62128009..62222878hg19UCSC Ensembl
Innerchr16:60685510..60780379hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3894870
hg1994870
hg1894870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559369
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)nsv1063685
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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