A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064327



Internal ID19153546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:73555450..73824057hg38UCSC Ensembl
Innerchr16:73589349..73857956hg19UCSC Ensembl
Innerchr16:72146850..72415457hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38268608
hg19268608
hg18268608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559573
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)nsv1064327
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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