A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557154



Internal ID18855435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12539061..12549098hg38UCSC Ensembl
Innerchr16:12632918..12642955hg19UCSC Ensembl
Innerchr16:12540419..12550456hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3810038
hg1910038
hg1810038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039338
Supporting Variants
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557154
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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