A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067178



Internal ID19156397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56160368..56188613hg38UCSC Ensembl
Innerchr16:56194280..56222525hg19UCSC Ensembl
Innerchr16:54751781..54780026hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3828246
hg1928246
hg1828246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559342, nssv3722713
Samples
Known GenesLOC283856
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067178
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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