A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557141



Internal ID18855422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11488714..11547571hg38UCSC Ensembl
Innerchr16:11582570..11641427hg19UCSC Ensembl
Innerchr16:11490071..11548928hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3858858
hg1958858
hg1858858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557141
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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