A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065916



Internal ID19155135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35224654..35526596hg38UCSC Ensembl
Innerchr16:34459025..34760967hg19UCSC Ensembl
Innerchr16:34316526..34618468hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38301943
hg19301943
hg18301943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3556082, nssv3722240, nssv3722241, nssv3556086, nssv3722237, nssv3556080, nssv3556081, nssv3556087, nssv3556084, nssv3556083, nssv3722239, nssv3722238, nssv3556085
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)nsv1065916
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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