A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061874



Internal ID19151093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35257653..35522700hg38UCSC Ensembl
Innerchr16:34492024..34757071hg19UCSC Ensembl
Innerchr16:34349525..34614572hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38265048
hg19265048
hg18265048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558961
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061874
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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