A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063057



Internal ID19152276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35495270hg38UCSC Ensembl
Innerchr16:34470704..34729641hg19UCSC Ensembl
Innerchr16:34328205..34587142hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38258938
hg19258938
hg18258938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558387, nssv3558388, nssv3558386, nssv3558389
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063057
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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