A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067027



Internal ID19156246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35323345..35505629hg38UCSC Ensembl
Innerchr16:34557716..34740000hg19UCSC Ensembl
Innerchr16:34415217..34597501hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38182285
hg19182285
hg18182285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2968n100
Supporting Variantsnssv3722674, nssv3559106
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)nsv1067027
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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