A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055333



Internal ID19144552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35501842hg38UCSC Ensembl
Innerchr16:34466559..34736213hg19UCSC Ensembl
Innerchr16:34324060..34593714hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38269655
hg19269655
hg18269655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3556155, nssv3556152, nssv3556153, nssv3722254, nssv3722253, nssv3722256, nssv3722255, nssv3556154
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)nsv1055333
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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