A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064724



Internal ID19153943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63250134..63362456hg38UCSC Ensembl
Innerchr16:63284038..63396360hg19UCSC Ensembl
Innerchr16:61841539..61953861hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38112323
hg19112323
hg18112323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2991n100
Supporting Variantsnssv3559374
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)nsv1064724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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